disulfiram
Generic: disulfiram
Labeler: sigmapharm laboratories, llcDrug Facts
Product Profile
Brand Name
disulfiram
Generic Name
disulfiram
Labeler
sigmapharm laboratories, llc
Dosage Form
TABLET
Routes
Active Ingredients
disulfiram 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42794-029
Product ID
42794-029_20208d67-134d-2cc1-e063-6394a90a59be
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091619
Listing Expiration
2026-12-31
Marketing Start
2022-01-11
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42794029
Hyphenated Format
42794-029
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
disulfiram (source: ndc)
Generic Name
disulfiram (source: ndc)
Application Number
ANDA091619 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (42794-029-08)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "20208d67-134d-2cc1-e063-6394a90a59be", "openfda": {"nui": ["N0000000183", "N0000175679"], "upc": ["0342794028083"], "unii": ["TR3MLJ1UAI"], "rxcui": ["197623", "197624"], "spl_set_id": ["40f5497f-fe84-43b2-8ff4-32d59edf3917"], "pharm_class_epc": ["Aldehyde Dehydrogenase Inhibitor [EPC]"], "pharm_class_moa": ["Acetyl Aldehyde Dehydrogenase Inhibitors [MoA]"], "manufacturer_name": ["Sigmapharm Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (42794-029-08)", "package_ndc": "42794-029-08", "marketing_start_date": "20220111"}], "brand_name": "Disulfiram", "product_id": "42794-029_20208d67-134d-2cc1-e063-6394a90a59be", "dosage_form": "TABLET", "pharm_class": ["Acetyl Aldehyde Dehydrogenase Inhibitors [MoA]", "Aldehyde Dehydrogenase Inhibitor [EPC]"], "product_ndc": "42794-029", "generic_name": "Disulfiram", "labeler_name": "Sigmapharm Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Disulfiram", "active_ingredients": [{"name": "DISULFIRAM", "strength": "500 mg/1"}], "application_number": "ANDA091619", "marketing_category": "ANDA", "marketing_start_date": "20220111", "listing_expiration_date": "20261231"}