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Bromocriptine Mesylate
Bromocriptine Mesylate - 0378-2042-01 - (bromocriptine mesylate)
Drug Information of Bromocriptine Mesylate
| Product NDC: | 0378-2042 |
| Proprietary Name: | Bromocriptine Mesylate |
| Non Proprietary Name: | bromocriptine mesylate |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; bromocriptine mesylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bromocriptine Mesylate
| Product NDC: | 0378-2042 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076962 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110504 |
Package Information of Bromocriptine Mesylate
| Package NDC: | 0378-2042-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0378-2042-01) |
NDC Information of Bromocriptine Mesylate
| NDC Code | 0378-2042-01 |
| Proprietary Name | Bromocriptine Mesylate |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0378-2042-01) |
| Product NDC | 0378-2042 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bromocriptine mesylate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110504 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | BROMOCRIPTINE MESYLATE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Ergolines [Chemical/Ingredient],Ergot Derivative [EPC] |
