acetaminophen

Generic: acetaminophen

Labeler: bluepoint laboratories
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler bluepoint laboratories
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-495
Product ID 68001-495_1a273bc1-09a5-3877-e063-6394a90a9388
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207229
Listing Expiration 2026-12-31
Marketing Start 2021-04-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68001495
Hyphenated Format 68001-495

Supplemental Identifiers

RxCUI
1148399
UPC
0368001495004
UNII
362O9ITL9D

Packaging Origin

Original Packager
true

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
  • 1 BOTTLE in 1 CARTON (68001-495-00) / 100 TABLET in 1 BOTTLE
source: ndc

Packages (1)

68001-495-00 1 BOTTLE in 1 CARTON (68001-495-00) / 100 TABLET in 1 BOTTLE

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": "1a273bc1-09a5-3877-e063-6394a90a9388", "openfda": {"upc": ["0368001495004"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["c065c531-88f5-0930-e053-2a95a90ae861"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68001-495-00)  / 100 TABLET in 1 BOTTLE", "package_ndc": "68001-495-00", "marketing_start_date": "20210430"}], "brand_name": "Acetaminophen", "product_id": "68001-495_1a273bc1-09a5-3877-e063-6394a90a9388", "dosage_form": "TABLET", "product_ndc": "68001-495", "generic_name": "Acetaminophen", "labeler_name": "BluePoint Laboratories", "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": "20210430", "listing_expiration_date": "20261231"}