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Bromocriptine Mesylate
Bromocriptine Mesylate - 0781-2119-01 - (bromocriptine mesylate)
Drug Information of Bromocriptine Mesylate
| Product NDC: | 0781-2119 |
| 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: | 0781-2119 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017962 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19780628 |
Package Information of Bromocriptine Mesylate
| Package NDC: | 0781-2119-01 |
| Package Description: | 100 CAPSULE in 1 PACKAGE (0781-2119-01) |
NDC Information of Bromocriptine Mesylate
| NDC Code | 0781-2119-01 |
| Proprietary Name | Bromocriptine Mesylate |
| Package Description | 100 CAPSULE in 1 PACKAGE (0781-2119-01) |
| Product NDC | 0781-2119 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bromocriptine mesylate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19780628 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Sandoz Inc |
| Substance Name | BROMOCRIPTINE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Ergolines [Chemical/Ingredient],Ergot Derivative [EPC] |
