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Cafergot
Cafergot - 0781-5405-01 - (Ergotamine Tartrate and Caffeine)
Drug Information of Cafergot
| Product NDC: | 0781-5405 |
| Proprietary Name: | Cafergot |
| Non Proprietary Name: | Ergotamine Tartrate and Caffeine |
| Active Ingredient(s): | 100; 1 mg/1; mg/1 & nbsp; Ergotamine Tartrate and Caffeine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cafergot
| Product NDC: | 0781-5405 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084294 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19820101 |
Package Information of Cafergot
| Package NDC: | 0781-5405-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0781-5405-01) |
NDC Information of Cafergot
| NDC Code | 0781-5405-01 |
| Proprietary Name | Cafergot |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0781-5405-01) |
| Product NDC | 0781-5405 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ergotamine Tartrate and Caffeine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19820101 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | CAFFEINE; ERGOTAMINE TARTRATE |
| Strength Number | 100; 1 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Ergotamine Derivative [EPC],Ergotamines [Chemical/Ingredient],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |
