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Pramipexole Dihydrochloride
Pramipexole Dihydrochloride - 63739-535-10 - (Pramipexole Dihydrochloride)
Drug Information of Pramipexole Dihydrochloride
| Product NDC: | 63739-535 |
| Proprietary Name: | Pramipexole Dihydrochloride |
| Non Proprietary Name: | Pramipexole Dihydrochloride |
| Active Ingredient(s): | .5 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: | 63739-535 |
| Labeler Name: | McKesson Packaging Services a business unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091254 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120622 |
Package Information of Pramipexole Dihydrochloride
| Package NDC: | 63739-535-10 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-535-10) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Pramipexole Dihydrochloride
| NDC Code | 63739-535-10 |
| Proprietary Name | Pramipexole Dihydrochloride |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-535-10) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 63739-535 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pramipexole Dihydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120622 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Packaging Services a business unit of McKesson Corporation |
| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
| Strength Number | .5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
