pramipexole dihydrochloride

Generic: pramipexole dihydrochloride

Labeler: golden state medical supply, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pramipexole dihydrochloride
Generic Name pramipexole dihydrochloride
Labeler golden state medical supply, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pramipexole dihydrochloride 1 mg/1

Manufacturer
Golden State Medical Supply, Inc.

Identifiers & Regulatory

Product NDC 60429-089
Product ID 60429-089_494fcbc6-e427-a591-e063-6394a90ae5df
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203855
Listing Expiration 2027-12-31
Marketing Start 2014-10-28

Pharmacologic Class

Classes
dopamine agonists [moa] nonergot dopamine agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60429089
Hyphenated Format 60429-089

Supplemental Identifiers

RxCUI
858625 859033 859040 859044 859048 859052
UNII
3D867NP06J

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 ANDA203855 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (60429-089-90)
source: ndc

Packages (1)

60429-089-90 90 TABLET in 1 BOTTLE (60429-089-90)

Ingredients (1)

pramipexole dihydrochloride (1 mg/1)

Linked Drug Pages (1)

Pramipexole Dihydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "494fcbc6-e427-a591-e063-6394a90ae5df", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["858625", "859033", "859040", "859044", "859048", "859052"], "spl_set_id": ["f8ac759f-59fb-49e4-a772-4114facdaea3"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (60429-089-90)", "package_ndc": "60429-089-90", "marketing_start_date": "20250407"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "60429-089_494fcbc6-e427-a591-e063-6394a90ae5df", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "60429-089", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA203855", "marketing_category": "ANDA", "marketing_start_date": "20141028", "listing_expiration_date": "20271231"}