Home
>
National Drug Code (NDC)
>
Pramipexole Dihydrochloride
Pramipexole Dihydrochloride - 51991-629-90 - (Pramipexole Dihydrochloride)
Drug Information of Pramipexole Dihydrochloride
| Product NDC: | 51991-629 |
| Proprietary Name: | Pramipexole Dihydrochloride |
| Non Proprietary Name: | Pramipexole Dihydrochloride |
| Active Ingredient(s): | .25 mg/1 & nbsp; Pramipexole Dihydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pramipexole Dihydrochloride
| Product NDC: | 51991-629 |
| Labeler Name: | Breckenridge Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091450 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101009 |
Package Information of Pramipexole Dihydrochloride
| Package NDC: | 51991-629-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (51991-629-90) |
NDC Information of Pramipexole Dihydrochloride
| NDC Code | 51991-629-90 |
| Proprietary Name | Pramipexole Dihydrochloride |
| Package Description | 90 TABLET in 1 BOTTLE (51991-629-90) |
| Product NDC | 51991-629 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pramipexole Dihydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101009 |
| Marketing Category Name | ANDA |
| Labeler Name | Breckenridge Pharmaceutical, Inc. |
| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
| Strength Number | .25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
