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Pramipexole Dihydrochloride
Pramipexole Dihydrochloride - 51079-576-20 - (pramipexole dihydrochloride)
Drug Information of Pramipexole Dihydrochloride
| Product NDC: | 51079-576 |
| Proprietary Name: | Pramipexole Dihydrochloride |
| Non Proprietary Name: | pramipexole dihydrochloride |
| Active Ingredient(s): | .125 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: | 51079-576 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077854 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101117 |
Package Information of Pramipexole Dihydrochloride
| Package NDC: | 51079-576-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-576-20) > 1 TABLET in 1 BLISTER PACK (51079-576-01) |
NDC Information of Pramipexole Dihydrochloride
| NDC Code | 51079-576-20 |
| Proprietary Name | Pramipexole Dihydrochloride |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-576-20) > 1 TABLET in 1 BLISTER PACK (51079-576-01) |
| Product NDC | 51079-576 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | pramipexole dihydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101117 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
| Strength Number | .125 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
