acetaminophen

Generic: acetaminophen

Labeler: american health packaging
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-924
Product ID 60687-924_4a0449b1-7dd9-f323-e063-6294a90ac587
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207229
Listing Expiration 2027-12-31
Marketing Start 2026-02-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687924
Hyphenated Format 60687-924

Supplemental Identifiers

RxCUI
1148399
UNII
362O9ITL9D

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 ANDA207229 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 30 BLISTER PACK in 1 CARTON (60687-924-21) / 1 TABLET in 1 BLISTER PACK (60687-924-11)
source: ndc

Packages (1)

60687-924-21 30 BLISTER PACK in 1 CARTON (60687-924-21) / 1 TABLET in 1 BLISTER PACK (60687-924-11)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a0449b1-7dd9-f323-e063-6294a90ac587", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["88e5345a-f240-473c-b329-2b0aa5f081f9"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-924-21)  / 1 TABLET in 1 BLISTER PACK (60687-924-11)", "package_ndc": "60687-924-21", "marketing_start_date": "20260201"}], "brand_name": "Acetaminophen", "product_id": "60687-924_4a0449b1-7dd9-f323-e063-6294a90ac587", "dosage_form": "TABLET", "product_ndc": "60687-924", "generic_name": "Acetaminophen", "labeler_name": "American Health Packaging", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA207229", "marketing_category": "ANDA", "marketing_start_date": "20260201", "listing_expiration_date": "20271231"}