penicillamine
Generic: penicillamine
Labeler: granules pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
penicillamine
Generic Name
penicillamine
Labeler
granules pharmaceuticals inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
penicillamine 250 mg/1
Manufacturer
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)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70010907
Hyphenated Format
70010-907
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (70010-907-01)
Packages (1)
Ingredients (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"}