penicillamine

Generic: penicillamine

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name penicillamine
Generic Name penicillamine
Labeler proficient rx lp
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

penicillamine 250 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-916
Product ID 71205-916_125ca13e-9784-45be-847a-6fdf9875bd6a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211735
Listing Expiration 2026-12-31
Marketing Start 2020-12-21

Pharmacologic Class

Established (EPC)
antirheumatic agent [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205916
Hyphenated Format 71205-916

Supplemental Identifiers

RxCUI
198070
UPC
0371205916008
UNII
GNN1DV99GX
NUI
N0000175713

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 ANDA211735 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (71205-916-00)
source: ndc

Packages (1)

71205-916-00 100 CAPSULE in 1 BOTTLE (71205-916-00)

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": "125ca13e-9784-45be-847a-6fdf9875bd6a", "openfda": {"nui": ["N0000175713"], "upc": ["0371205916008"], "unii": ["GNN1DV99GX"], "rxcui": ["198070"], "spl_set_id": ["c92335c6-f6fa-4768-9401-55c6b7f87699"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71205-916-00)", "package_ndc": "71205-916-00", "marketing_start_date": "20210708"}], "brand_name": "Penicillamine", "product_id": "71205-916_125ca13e-9784-45be-847a-6fdf9875bd6a", "dosage_form": "CAPSULE", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "71205-916", "generic_name": "Penicillamine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Penicillamine", "active_ingredients": [{"name": "PENICILLAMINE", "strength": "250 mg/1"}], "application_number": "ANDA211735", "marketing_category": "ANDA", "marketing_start_date": "20201221", "listing_expiration_date": "20261231"}