penicillamine

Generic: penicillamine

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

Drug Facts

Product Profile

Brand Name penicillamine
Generic Name penicillamine
Labeler granules pharmaceuticals inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

penicillamine 250 mg/1

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-907
Product ID 70010-907_2ff8270b-b31e-5b72-e063-6294a90acf7c
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 70010907
Hyphenated Format 70010-907

Supplemental Identifiers

RxCUI
198070
UPC
0370010907010
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 ANDA211735 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (70010-907-01)
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": "2ff8270b-b31e-5b72-e063-6294a90acf7c", "openfda": {"nui": ["N0000175713"], "upc": ["0370010907010"], "unii": ["GNN1DV99GX"], "rxcui": ["198070"], "spl_set_id": ["f658b20a-269f-4e78-a79b-a56a5ed8dc1b"], "pharm_class_epc": ["Antirheumatic Agent [EPC]"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (70010-907-01)", "package_ndc": "70010-907-01", "marketing_start_date": "20201221"}], "brand_name": "Penicillamine", "product_id": "70010-907_2ff8270b-b31e-5b72-e063-6294a90acf7c", "dosage_form": "CAPSULE", "pharm_class": ["Antirheumatic Agent [EPC]"], "product_ndc": "70010-907", "generic_name": "Penicillamine", "labeler_name": "Granules Pharmaceuticals Inc.", "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"}