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Pramipexole
Pramipexole - 57664-210-13 - (Pramipexole)
Drug Information of Pramipexole
| Product NDC: | 57664-210 |
| Proprietary Name: | Pramipexole |
| Non Proprietary Name: | Pramipexole |
| Active Ingredient(s): | .75 mg/1 & nbsp; Pramipexole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pramipexole
| Product NDC: | 57664-210 |
| Labeler Name: | Caraco Pharmaceutical Laboratories, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091683 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130523 |
Package Information of Pramipexole
| Package NDC: | 57664-210-13 |
| Package Description: | 500 TABLET in 1 BOTTLE (57664-210-13) |
NDC Information of Pramipexole
| NDC Code | 57664-210-13 |
| Proprietary Name | Pramipexole |
| Package Description | 500 TABLET in 1 BOTTLE (57664-210-13) |
| Product NDC | 57664-210 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pramipexole |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130523 |
| Marketing Category Name | ANDA |
| Labeler Name | Caraco Pharmaceutical Laboratories, Ltd. |
| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
| Strength Number | .75 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
