penicillamine

Generic: penicillamine

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name penicillamine
Generic Name penicillamine
Labeler actavis pharma, inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

penicillamine 250 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0591-4171
Product ID 0591-4171_24e42ecc-c15e-499d-85a9-bf4b5e277bea
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210976
Listing Expiration 2026-12-31
Marketing Start 2019-06-25

Pharmacologic Class

Established (EPC)
antirheumatic agent [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05914171
Hyphenated Format 0591-4171

Supplemental Identifiers

RxCUI
198070
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 ANDA210976 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (0591-4171-01)
source: ndc

Packages (1)

Ingredients (1)

penicillamine (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24e42ecc-c15e-499d-85a9-bf4b5e277bea", "openfda": {"nui": ["N0000175713"], "unii": ["GNN1DV99GX"], "rxcui": ["198070"], "spl_set_id": ["594d7a82-af1d-41c4-98ee-0ea6895fc237"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0591-4171-01)", "package_ndc": "0591-4171-01", "marketing_start_date": "20190625"}], "brand_name": "Penicillamine", "product_id": "0591-4171_24e42ecc-c15e-499d-85a9-bf4b5e277bea", "dosage_form": "CAPSULE", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "0591-4171", "generic_name": "Penicillamine", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Penicillamine", "active_ingredients": [{"name": "PENICILLAMINE", "strength": "250 mg/1"}], "application_number": "ANDA210976", "marketing_category": "ANDA", "marketing_start_date": "20190625", "listing_expiration_date": "20261231"}