penicillamine

Generic: penicillamine

Labeler: endo usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name penicillamine
Generic Name penicillamine
Labeler endo usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

penicillamine 250 mg/1

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 0254-2000
Product ID 0254-2000_fef4bc4f-65a5-42ae-89fb-64815448a62c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211196
Listing Expiration 2026-12-31
Marketing Start 2020-01-02

Pharmacologic Class

Established (EPC)
antirheumatic agent [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02542000
Hyphenated Format 0254-2000

Supplemental Identifiers

RxCUI
198071
UPC
0302542000013
UNII
GNN1DV99GX
NUI
N0000175713

Packaging Origin

Original Packager
true

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 penicillamine (source: ndc)
Generic Name penicillamine (source: ndc)
Application Number ANDA211196 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0254-2000-01)
source: ndc

Packages (1)

0254-2000-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0254-2000-01)

Ingredients (1)

penicillamine (250 mg/1)

Linked Drug Pages (1)

penicillamine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fef4bc4f-65a5-42ae-89fb-64815448a62c", "openfda": {"nui": ["N0000175713"], "upc": ["0302542000013"], "unii": ["GNN1DV99GX"], "rxcui": ["198071"], "spl_set_id": ["72ee469c-f9ef-4bb4-922f-5d71276664a5"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0254-2000-01)", "package_ndc": "0254-2000-01", "marketing_start_date": "20200102"}], "brand_name": "penicillamine", "product_id": "0254-2000_fef4bc4f-65a5-42ae-89fb-64815448a62c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "0254-2000", "generic_name": "penicillamine", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "penicillamine", "active_ingredients": [{"name": "PENICILLAMINE", "strength": "250 mg/1"}], "application_number": "ANDA211196", "marketing_category": "ANDA", "marketing_start_date": "20200102", "listing_expiration_date": "20261231"}