M/S Promise Pharmaceutical Labs Sagar

Licence No. 25/14/85 Valid Upto 31/12/2017 703 Rajakhedi Makroniya Sagar M.P. 1. Chlorpheniramine Maleate Tablets I.P . 4mg /Tab. 2. Ephedrine Hydrochloride Tablets I.P. 15mg/Tab. 3. Furazolidone Tablets I.P .100mg/Tab. 4. Aspirin Tablets I.P. 300mg/Tab. 5. Ibuprofen Tablets I.P. (Profen) Each Tablet Contains: Ibuprofen I.P. 400 mg

6. Metronidazole Tablets I.P. 200 Mg/Tab.

7.

Dicyclomine Hydrochloride And Paracetamol Tablets Coligesic Each Tablet Contains: Dicyclomine Hydrochloride I.P. Paracetamol I.P. Colour:Sunset Yellow 20 mg 325 mg

-----------------------------------------------------------------------------------------------------------------Condition :1. Pursuant To The Directions Contained In Govt Of India Ministry Of Health And Family Welfare , New Delhi Letter No. X11011/1/2011-Dfqc Dt. 1 Ict 2012 The Trade Names Of The Product Are Treated As Deleted. 2.The Licensee Shall Submit Data On Safety And Efficacy Of Those Permitted Items Of F.D.C Which Do Not Appear In The List Of Items Approved By D.C.G.I New Delhi, Within Eighteen Monts W.E.F 15.01.2013 3. The Licensee Shall Not Manufactre Any Drug Formulations Which Is Prohibited By Govt. Of India U/S 26 A Of The Drugs And Cosmetics Act. 1940 From Time To Time 4 Content Of Paracetamol Changed From 500 Mg. To 325 Mg As Per The Dcgi Letter No 18-6/2011- Dc Date 23.09.2011 Licensing Authority Food And Drug Administration Madhya Pradesh

8 Aluminium Hydroxide Gel . Magnesium Hydroxide And Methyl Polysiloxane Tablets (Allusil Mps) Each Tablet Contains Dried Aluminium Hydroxide Gel I.P. Magnesium Hydroxide N.F. Activated Methyl Polysiloxane I.P. Colour-Erythrosine/Sunset Yellow 250 mg 250 mg 10 mg

9 Acetyl Salicylic Acid . Paracetamol And Caffeine Tablets . (Paingo) Each Tablet Contains: Acetyl Salicylic Acid I.P. Paracetamol I.P. Caffeine (Anhydrous) I.P. 300 mg 150 mg 30 mg

10. Trimethoprim & Sulphamethoxazole Tablets I.P. (Sulfrim) Each Tablet Contains: Trimethoprim I.P. Sulphamethoxazole I.P. .11 Chloroquine Phosphate Tablets I.P. (Proquine) Each Tablet Contains: Chloroquine Phosphate I.P. 250 mg 80 mg 400 mg

Condition 1. Pursuant To The Directions Contained In Govt Of India Ministry Of Health And Family Welfare , New Delhi Laatter No. X11011/1/2011-Dfqc Dt. 1 Ict 2012 The Trade Names Of The Product Are Treated As Deleted. 2.The Licensee Shall Submit Data On Safety And Efficacy Of Those Permitted Items Of F.D.C Which Do Not Appear In The List Of Items Approved By D.C.G.I New Delhi, Within Eighteen Monts W.E.F 15.01.2013 3. The Licensee Shall Not Manufactre Any Drug Formulations Which Is Prohibited By Govt. Of India U/S 26 A Of The Drugs And Cosmetics Act. 1940 From Time To Time 4 Content Of Paracetamol Changed From 500 Mg. To 325 Mg As Per The Dcgi Latter No 18-6/2011- Dc Date 23.09.2011 Licensing Authority Food And Drug Administration Madhya Pradesh

12. Ibuprofen & Paracetamol Tablets (Cetafen) Each Tablet Contains: Ibuprofen I.P. Paracetamol I.P. 13 Acety Salicylic Acid . Paracetamol And Caffieine Tablets . (Painpro) Each Tablet Contains: Acetyl Salicylic Acid I.P. Paracetamol I.P. Caffeine Anhydrous I.P. .14 Paracetamol Tablets I.P. (Unimol) 15. Cotrimoxazole Tablets I.P. (Qutran D.S.) Each Tablet Contains: Trimethoprim I.P. Sulphamethoxazole I.P. 16. Ibuprofen & Paracetamol Tablets (Zeflam) Each Tablet Contains: Ibuprofen I.P. Paracetamol I.P. 400 mg 325 mg 160 mg 800 mg Each Tablet Contains: Paracetamol I.P. 325 mg 300 mg 150 mg 30 mg 400 mg 325 mg

Condition 1. Pursuant To The Directions Contained In Govt Of India Ministry Of Health And Family Welfare , New Delhi Letter No. X11011/1/2011-Dfqc Dt. 1 Ict 2012 The Trade Names Of The Product Are Treated As Deleted. 2.The Licensee Shall Submit Data On Safety And Efficacy Of Those Permitted Items Of F.D.C Which Do Not Appear In The List Of Items Approved By D.C.G.I New Delhi, Within Eighteen Monts W.E.F 15.01.2013 3. The Licensee Shall Not Manufactre Any Drug Formulations Which Is Prohibited By Govt. Of India U/S 26 A Of The Drugs And Cosmetics Act. 1940 From Time To Time 4 Content Of Paracetamol Changed From 500 Mg. To 325 Mg As Per The Dcgi Letter No 18-6/2011- Dc Date 23.09.2011 Licensing Authority Food And Drug Administration Madhya Pradesh

17 Phenylephrine Hydrochloride , Paracetamol And Chlorpheniramine Maleate Tablets . (Synrex) Each Tablet Contains: Phenylephrine Hydrochloride I.P. Paracetamol I.P. C.P.Maleate I.P. Caffeine Anhydrous I.P. 5 mg 325 mg 2 mg 16 mg

18 Dicyclomine Hydrochloride And Paracetamol Tablets . (Colin-D) Each Tablet Contains: Dicyclomine Hydrochloride I.P. Paracetamol I.P. Colour Erythrosine 19 Paracetamol And Diclofenec Sodium Tablets . (Topgesic) Each Tablet Contains: Paracetamol I.P. Diclofenec Sodium I.P. 20 Aluminium Hydroxide,Magnesium Hydroxide And Simethicone Tablets . (Allusil Forte) Each Tablet Contains: Dried Aluminum Hydroxide Gel I.P. Magnesium Hydroxide N.F. Simethicone Usp Colour-Tartrazine 250 mg 250 mg 50 mg 325 mg 50 mg 20 mg 325 mg

Condition 1. Pursuant To The Directions Contained In Govt Of India Ministry Of Health And Family Welfare , New Delhi Letter No. X11011/1/2011-Dfqc Dt. 1 Ict 2012 The Trade Names Of The Product Are Treated As Deleted. 2.The Licensee Shall Submit Data On Safety And Efficacy Of Those Permitted Items Of F.D.C Which Do Not Appear In The List Of Items Approved By D.C.G.I New Delhi, Within Eighteen Monts W.E.F 15.01.2013 3. The Licensee Shall Not Manufactre Any Drug Formulations Which Is Prohibited By Govt. Of India U/S 26 A Of The Drugs And Cosmetics Act. 1940 From Time To Time 4 Content Of Paracetamol Changed From 500 Mg. To 325 Mg As Per The Dcgi Letter No 18-6/2011- Dc Date 23.09.2011 Licensing Authority Food And Drug Administration Madhya Pradesh

21. Ciprofloxacin Tablets I.P. (Sip 500)

Each Tablet Contains: Ciprofloxacin Hydrochloride I.P. Equivalent To Ciprofloxacin Base--500 mg

22. Ciprofloxacin Tablets I.P. (Sip 250)

Each Tablet Contains: Ciprofloxacin Hydrochloride I.P. Equivalent To Ciprofloxacin Base--250 mg

23 Acetaminophen And Diclofenec Sodium Tablets . (Paracalm) Each Tablet Contains : Acetaminophen I.P. Diclofenec Sodium I.P. Colour- Tartrazine 24 Peracetamol And Diclofenec Sodium Tablets . (Butapam dp ) Each Tablet Contains: Paracetamol I.P. Diclofenec Sodium I.P. Colour-Erythrosine 25 Bromhexine Hydrochloride ,Ephedrine Hyodrochloriede & Chlorpheniramine Maleate Tablets . ( Copex ) Each Tablet Contains: Bromhexine Hydrochloride B.P. Ephedrine Hydrochloride I.P. Chlorpheniramine Maleate I.P. 8 mg 15 mg 4 mg 325 mg 50 mg 325 mg 50 mg

Condition 1. Pursuant To The Directions Contained In Govt Of India Ministry Of Health And Family Welfare , New Delhi Letter No. X11011/1/2011-Dfqc Dt. 1 Ict 2012 The Trade Names Of The Product Are Treated As Deleted. 2.The Licensee Shall Submit Data On Safety And Efficacy Of Those Permitted Items Of F.D.C Which Do Not Appear In The List Of Items Approved By D.C.G.I New Delhi, Within Eighteen Monts W.E.F 15.01.2013 3. The Licensee Shall Not Manufactre Any Drug Formulations Which Is Prohibited By Govt. Of India U/S 26 A Of The Drugs And Cosmetics Act. 1940 From Time To Time 4 Content Of Paracetamol Changed From 500 Mg. To 325 Mg As Per The Dcgi Letter No 18-6/2011- Dc Date 23.09.2011 Licensing Authority Food And Drug Administration Madhya Pradesh

.26 Nimesulide Tablets (Megesic) . (Diclopam )

Each Tablet Contains: Nimesulide B.P 100 mg

27 Paracetamol & Diclofenec Sodium Tablets Each Tablet Contains: Paracetamol I.P. Diclofenec Sodium I.P. 28 Diclofenec Sodium , Paracetamol And Magnesium Trisilicate Tablets . (Diclopam Plus ) Each Tablet Contains: Diclofenec Sodium I.P. Paracetamol I.P. Magnesium Trisilicate I.P. 29 Paracetamol , Diclfenec Sodium And Chlorzoxazone Tablets . (Paracalm O ) Each Tablet Contains: Paracetamol I.P. Diclofenec Sodium I.P. Chlorzoxazone U.S.P. 30 Tinidazole & Ciprofloxacin Hydrochloride Tablets .(Sip-Tz- Forte ) Each Tablet Contains: Tinidazole I.P. Ciprofloxacin Hydrochloride I.P. Equivalent To Ciprofloxacin Base 31. Furazolidone & Metronidazole Tablets (Fuzo Plus) Each Tablet Contains: Furazolidone I.P. Metronidazole I.P. 32 Diclofenec Potassium And Paracetamol Tablets . (D-Pan) Each Tablet Contains: Diclofenec Potassium I.P. Paracetamol I.P.
Condition 1. Pursuant To The Directions Contained In Govt Of India Ministry Of Health And Family Welfare , New Delhi Letter No. X11011/1/2011-Dfqc Dt. 1 Ict 2012 The Trade Names Of The Product Are Treated As Deleted. 2.The Licensee Shall Submit Data On Safety And Efficacy Of Those Permitted Items Of F.D.C Which Do Not Appear In The List Of Items Approved By D.C.G.I New Delhi, Within Eighteen Monts W.E.F 15.01.2013 3. The Licensee Shall Not Manufactre Any Drug Formulations Which Is Prohibited By Govt. Of India U/S 26 A Of The Drugs And Cosmetics Act. 1940 From Time To Time 4 Content Of Paracetamol Changed From 500 Mg. To 325 Mg As Per The Dcgi Letter No 18-6/2011- Dc Date 23.09.2011 Licensing Authority Food And Drug Administration Madhya Pradesh

325 mg 50 mg

50 mg 325 mg 100 mg

325 mg 50 mg 250 mg

600 mg 500 mg

100 mg 300 mg

50 mg 325 mg