acetaminophen and codeine phosphate
Generic: acetaminophen and codeine phosphate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
acetaminophen and codeine phosphate
Generic Name
acetaminophen and codeine phosphate
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 300 mg/1, codeine phosphate 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4104
Product ID
70518-4104_3fa4b8cd-a67b-1f48-e063-6294a90a04e3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089805
DEA Schedule
ciii
Listing Expiration
2026-12-31
Marketing Start
2024-06-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184104
Hyphenated Format
70518-4104
Supplemental Identifiers
RxCUI
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
- 30 TABLET in 1 BLISTER PACK (70518-4104-0)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fa4b8cd-a67b-1f48-e063-6294a90a04e3", "openfda": {"unii": ["362O9ITL9D", "GSL05Y1MN6"], "rxcui": ["993781"], "spl_set_id": ["40d4a71e-341e-48b3-b925-ba35b7910dff"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4104-0)", "package_ndc": "70518-4104-0", "marketing_start_date": "20240617"}], "brand_name": "Acetaminophen and Codeine Phosphate", "product_id": "70518-4104_3fa4b8cd-a67b-1f48-e063-6294a90a04e3", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "70518-4104", "dea_schedule": "CIII", "generic_name": "Acetaminophen and Codeine Phosphate", "labeler_name": "REMEDYREPACK 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": "20240617", "listing_expiration_date": "20261231"}