| Product NDC: | 0574-0106 |
| 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) |
| Product NDC: | 0574-0106 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077646 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081001 |
| Package NDC: | 0574-0106-01 |
| Package Description: | 24 BOTTLE in 1 CARTON (0574-0106-01) > 100 TABLET in 1 BOTTLE |
| NDC Code | 0574-0106-01 |
| Proprietary Name | Bromocriptine mesylate |
| Package Description | 24 BOTTLE in 1 CARTON (0574-0106-01) > 100 TABLET in 1 BOTTLE |
| Product NDC | 0574-0106 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Bromocriptine mesylate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20081001 |
| Marketing Category Name | ANDA |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | BROMOCRIPTINE MESYLATE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Ergolines [Chemical/Ingredient],Ergot Derivative [EPC] |