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PRAMIPEXOLE DIHYDROCHLORIDE
PRAMIPEXOLE DIHYDROCHLORIDE - 68382-197-05 - (PRAMIPEXOLE DIHYDROCHLORIDE)
Drug Information of PRAMIPEXOLE DIHYDROCHLORIDE
| Product NDC: | 68382-197 |
| 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: | 68382-197 |
| Labeler Name: | Zydus Pharmaceuticals (USA) Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078920 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100710 |
Package Information of PRAMIPEXOLE DIHYDROCHLORIDE
| Package NDC: | 68382-197-05 |
| Package Description: | 500 TABLET in 1 BOTTLE (68382-197-05) |
NDC Information of PRAMIPEXOLE DIHYDROCHLORIDE
| NDC Code | 68382-197-05 |
| Proprietary Name | PRAMIPEXOLE DIHYDROCHLORIDE |
| Package Description | 500 TABLET in 1 BOTTLE (68382-197-05) |
| Product NDC | 68382-197 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PRAMIPEXOLE DIHYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100710 |
| Marketing Category Name | ANDA |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE |
| Strength Number | .25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |
