pramipexole dihydrochloride

Generic: pramipexole dihydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pramipexole dihydrochloride
Generic Name pramipexole dihydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pramipexole dihydrochloride .25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3280
Product ID 50090-3280_f192c472-528a-4328-ac85-1e2c27eb8c78
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202633
Listing Expiration 2026-12-31
Marketing Start 2012-10-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500903280
Hyphenated Format 50090-3280

Supplemental Identifiers

RxCUI
859040 859044
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 ANDA202633 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-3280-0)
source: ndc

Packages (1)

50090-3280-0 90 TABLET in 1 BOTTLE (50090-3280-0)

Ingredients (1)

pramipexole dihydrochloride (.25 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": "f192c472-528a-4328-ac85-1e2c27eb8c78", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859040", "859044"], "spl_set_id": ["29b639e3-25a5-4c2f-b4ea-a119db79fe0c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-3280-0)", "package_ndc": "50090-3280-0", "marketing_start_date": "20171127"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "50090-3280_f192c472-528a-4328-ac85-1e2c27eb8c78", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "50090-3280", "generic_name": "Pramipexole Dihydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pramipexole Dihydrochloride", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".25 mg/1"}], "application_number": "ANDA202633", "marketing_category": "ANDA", "marketing_start_date": "20121026", "listing_expiration_date": "20261231"}