pramipexole dihydrochloride
Generic: pramipexole dihydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
pramipexole dihydrochloride
Generic Name
pramipexole dihydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
pramipexole dihydrochloride 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-8289
Product ID
63629-8289_e0c596d9-a2a0-42bd-a987-7d3d8df3488b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202633
Listing Expiration
2026-12-31
Marketing Start
2012-10-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636298289
Hyphenated Format
63629-8289
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
pramipexole dihydrochloride (source: ndc)
Generic Name
pramipexole dihydrochloride (source: ndc)
Application Number
ANDA202633 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (63629-8289-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e0c596d9-a2a0-42bd-a987-7d3d8df3488b", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859052"], "spl_set_id": ["1ebb3e0b-8fd5-4ac8-ba2f-abfcfc0c91ad"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-8289-1)", "package_ndc": "63629-8289-1", "marketing_start_date": "20200110"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "63629-8289_e0c596d9-a2a0-42bd-a987-7d3d8df3488b", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "63629-8289", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA202633", "marketing_category": "ANDA", "marketing_start_date": "20121026", "listing_expiration_date": "20261231"}