pramipexole dihydrochloride

Generic: pramipexole dihydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pramipexole dihydrochloride
Generic Name pramipexole dihydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pramipexole dihydrochloride 1.5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1504
Product ID 71335-1504_b9f0ffda-1cd2-47c8-85f5-3e61a567f207
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 713351504
Hyphenated Format 71335-1504

Supplemental Identifiers

RxCUI
859048
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
  • 1.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1504-1)
  • 90 TABLET in 1 BOTTLE (71335-1504-2)
source: ndc

Packages (2)

71335-1504-1 30 TABLET in 1 BOTTLE (71335-1504-1) 71335-1504-2 90 TABLET in 1 BOTTLE (71335-1504-2)

Ingredients (1)

pramipexole dihydrochloride (1.5 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": "b9f0ffda-1cd2-47c8-85f5-3e61a567f207", "openfda": {"unii": ["3D867NP06J"], "rxcui": ["859048"], "spl_set_id": ["422b27af-5e7d-4fe1-81bc-ed545c26b476"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1504-1)", "package_ndc": "71335-1504-1", "marketing_start_date": "20211228"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1504-2)", "package_ndc": "71335-1504-2", "marketing_start_date": "20200211"}], "brand_name": "Pramipexole Dihydrochloride", "product_id": "71335-1504_b9f0ffda-1cd2-47c8-85f5-3e61a567f207", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "71335-1504", "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": "1.5 mg/1"}], "application_number": "ANDA202633", "marketing_category": "ANDA", "marketing_start_date": "20121026", "listing_expiration_date": "20261231"}