acetaminophen and codeine phosphate
Generic: acetaminophen and codeine phosphate
Labeler: nucare pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
acetaminophen and codeine phosphate
Generic Name
acetaminophen and codeine phosphate
Labeler
nucare pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 300 mg/1, codeine phosphate 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3824
Product ID
68071-3824_31d24074-fc9e-6c3b-e063-6294a90a7b07
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089805
DEA Schedule
ciii
Listing Expiration
2026-12-31
Marketing Start
2024-05-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713824
Hyphenated Format
68071-3824
Supplemental Identifiers
RxCUI
UPC
UNII
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
acetaminophen and codeine phosphate (source: ndc)
Generic Name
acetaminophen and codeine phosphate (source: ndc)
Application Number
ANDA089805 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
- 30 mg/1
Packaging
- 6 TABLET in 1 BOTTLE (68071-3824-6)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31d24074-fc9e-6c3b-e063-6294a90a7b07", "openfda": {"upc": ["0368071382464"], "unii": ["362O9ITL9D", "GSL05Y1MN6"], "rxcui": ["993781"], "spl_set_id": ["31d24067-3c25-0f1a-e063-6394a90a9f1d"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BOTTLE (68071-3824-6)", "package_ndc": "68071-3824-6", "marketing_start_date": "20250402"}], "brand_name": "Acetaminophen and Codeine Phosphate", "product_id": "68071-3824_31d24074-fc9e-6c3b-e063-6294a90a7b07", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-3824", "dea_schedule": "CIII", "generic_name": "Acetaminophen and Codeine Phosphate", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetaminophen and Codeine Phosphate", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "CODEINE PHOSPHATE", "strength": "30 mg/1"}], "application_number": "ANDA089805", "marketing_category": "ANDA", "marketing_start_date": "20240520", "listing_expiration_date": "20261231"}