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Bromocriptine mesylate
Bromocriptine mesylate - 68382-110-06 - (Bromocriptine mesylate)
Drug Information of Bromocriptine mesylate
| Product NDC: | 68382-110 |
| Proprietary Name: | Bromocriptine mesylate |
| Non Proprietary Name: | Bromocriptine mesylate |
| Active Ingredient(s): | 5 mg/1 & nbsp; Bromocriptine mesylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bromocriptine mesylate
| Product NDC: | 68382-110 |
| Labeler Name: | Zydus Pharmaceuticals (USA) Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078899 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090123 |
Package Information of Bromocriptine mesylate
| Package NDC: | 68382-110-06 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (68382-110-06) |
NDC Information of Bromocriptine mesylate
| NDC Code | 68382-110-06 |
| Proprietary Name | Bromocriptine mesylate |
| Package Description | 30 CAPSULE in 1 BOTTLE (68382-110-06) |
| Product NDC | 68382-110 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Bromocriptine mesylate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090123 |
| Marketing Category Name | ANDA |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| Substance Name | BROMOCRIPTINE MESYLATE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Ergolines [Chemical/Ingredient],Ergot Derivative [EPC] |
