| Product NDC: | 13668-093 | 
| 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) | 
| Product NDC: | 13668-093 | 
| Labeler Name: | Torrent Pharmaceuticals Limited | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA090865 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20101008 | 
| Package NDC: | 13668-093-90 | 
| Package Description: | 90 TABLET in 1 BOTTLE (13668-093-90) | 
| NDC Code | 13668-093-90 | 
| Proprietary Name | Pramipexole Dihydrochloride | 
| Package Description | 90 TABLET in 1 BOTTLE (13668-093-90) | 
| Product NDC | 13668-093 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Pramipexole Dihydrochloride | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20101008 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Torrent Pharmaceuticals Limited | 
| Substance Name | PRAMIPEXOLE DIHYDROCHLORIDE | 
| Strength Number | .5 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC] |