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 60 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-4749
Product ID
68071-4749_1adb4174-34af-5df8-e063-6294a90aa62b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202800
DEA Schedule
ciii
Listing Expiration
2026-12-31
Marketing Start
2013-04-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680714749
Hyphenated Format
68071-4749
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
ANDA202800 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
- 60 mg/1
Packaging
- 60 TABLET in 1 BOTTLE (68071-4749-6)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1adb4174-34af-5df8-e063-6294a90aa62b", "openfda": {"upc": ["0368071474961"], "unii": ["362O9ITL9D", "GSL05Y1MN6"], "rxcui": ["993890"], "spl_set_id": ["80c9a58d-98ae-5497-e053-2991aa0a61fb"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-4749-6)", "package_ndc": "68071-4749-6", "marketing_start_date": "20190131"}], "brand_name": "Acetaminophen and Codeine Phosphate", "product_id": "68071-4749_1adb4174-34af-5df8-e063-6294a90aa62b", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-4749", "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": "60 mg/1"}], "application_number": "ANDA202800", "marketing_category": "ANDA", "marketing_start_date": "20130415", "listing_expiration_date": "20261231"}