penicillamine

Generic: penicillamine

Labeler: lupin pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name penicillamine
Generic Name penicillamine
Labeler lupin pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

penicillamine 250 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 70748-153
Product ID 70748-153_99f3ca78-1663-47a1-9ed3-9c4eaa9f0271
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212933
Listing Expiration 2026-12-31
Marketing Start 2021-03-01

Pharmacologic Class

Established (EPC)
antirheumatic agent [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70748153
Hyphenated Format 70748-153

Supplemental Identifiers

RxCUI
198071
UPC
0370748153017
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 ANDA212933 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70748-153-01)
source: ndc

Packages (1)

70748-153-01 100 TABLET in 1 BOTTLE (70748-153-01)

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": "99f3ca78-1663-47a1-9ed3-9c4eaa9f0271", "openfda": {"nui": ["N0000175713"], "upc": ["0370748153017"], "unii": ["GNN1DV99GX"], "rxcui": ["198071"], "spl_set_id": ["f6ecaf47-902f-4378-b524-7a88f20ba138"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70748-153-01)", "package_ndc": "70748-153-01", "marketing_start_date": "20210301"}], "brand_name": "Penicillamine", "product_id": "70748-153_99f3ca78-1663-47a1-9ed3-9c4eaa9f0271", "dosage_form": "TABLET", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "70748-153", "generic_name": "Penicillamine", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Penicillamine", "active_ingredients": [{"name": "PENICILLAMINE", "strength": "250 mg/1"}], "application_number": "ANDA212933", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}