acetaminophen
Generic: acetaminophen
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
acetaminophen
Generic Name
acetaminophen
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen .5 g/g
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1666
Product ID
51662-1666_35478de8-50d1-5d0a-e063-6294a90a88ba
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M013
Listing Expiration
2026-12-31
Marketing Start
2020-01-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621666
Hyphenated Format
51662-1666
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 (source: ndc)
Generic Name
acetaminophen (source: ndc)
Application Number
M013 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 g/g
Packaging
- 2 POUCH in 1 PACKET (51662-1666-2) / .5 g in 1 POUCH
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35478de8-50d1-5d0a-e063-6294a90a88ba", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["35478de8-50d0-5d0a-e063-6294a90a88ba"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "2 POUCH in 1 PACKET (51662-1666-2) / .5 g in 1 POUCH", "package_ndc": "51662-1666-2", "marketing_start_date": "20200130"}], "brand_name": "ACETAMINOPHEN", "product_id": "51662-1666_35478de8-50d1-5d0a-e063-6294a90a88ba", "dosage_form": "TABLET", "product_ndc": "51662-1666", "generic_name": "ACETAMINOPHEN", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": ".5 g/g"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200130", "listing_expiration_date": "20261231"}