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Parlodel
Parlodel - 0078-0017-15 - (bromocriptine mesylate)
Drug Information of Parlodel
| Product NDC: | 0078-0017 |
| Proprietary Name: | Parlodel |
| 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 Parlodel
| Product NDC: | 0078-0017 |
| Labeler Name: | Novartis Pharmaceuticals Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017962 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19780628 |
Package Information of Parlodel
| Package NDC: | 0078-0017-15 |
| Package Description: | 30 TABLET in 1 PACKAGE (0078-0017-15) |
NDC Information of Parlodel
| NDC Code | 0078-0017-15 |
| Proprietary Name | Parlodel |
| Package Description | 30 TABLET in 1 PACKAGE (0078-0017-15) |
| Product NDC | 0078-0017 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bromocriptine mesylate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19780628 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Pharmaceuticals Corporation |
| Substance Name | BROMOCRIPTINE MESYLATE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Ergolines [Chemical/Ingredient],Ergot Derivative [EPC] |
