acetaminophen

Generic: acetaminophen

Labeler: time cap laboratories, inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH NOT FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler time cap laboratories, inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
TIME CAP LABORATORIES, INC

Identifiers & Regulatory

Product NDC 49483-342
Product ID 49483-342_7d3e2e18-1dee-4000-e053-2a91aa0aeefe
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH NOT FINAL
Application Number part343
Listing Expiration 2026-12-31
Marketing Start 2012-05-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49483342
Hyphenated Format 49483-342

Supplemental Identifiers

RxCUI
198440
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 part343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100000 TABLET, FILM COATED in 1 CARTON (49483-342-00)
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-342-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-342-10)
source: ndc

Packages (3)

49483-342-00 100000 TABLET, FILM COATED in 1 CARTON (49483-342-00) 49483-342-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-342-01) 49483-342-10 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-342-10)

Ingredients (1)

acetaminophen (500 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": "7d3e2e18-1dee-4000-e053-2a91aa0aeefe", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["2569383a-4a05-4ddb-852e-b37e487ffcde"], "manufacturer_name": ["TIME CAP LABORATORIES, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100000 TABLET, FILM COATED in 1 CARTON (49483-342-00)", "package_ndc": "49483-342-00", "marketing_start_date": "20181217"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-342-01)", "package_ndc": "49483-342-01", "marketing_start_date": "20181217"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-342-10)", "package_ndc": "49483-342-10", "marketing_start_date": "20181217"}], "brand_name": "ACETAMINOPHEN", "product_id": "49483-342_7d3e2e18-1dee-4000-e053-2a91aa0aeefe", "dosage_form": "TABLET, FILM COATED", "product_ndc": "49483-342", "generic_name": "ACETAMINOPHEN", "labeler_name": "TIME CAP LABORATORIES, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "part343", "marketing_category": "OTC MONOGRAPH NOT FINAL", "marketing_start_date": "20120501", "listing_expiration_date": "20261231"}