extra strength acetaminophen

Generic: acetaminophen

Labeler: time cap laboratories, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name extra strength acetaminophen
Generic Name acetaminophen
Labeler time cap laboratories, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
TIME CAP LABORATORIES, INC.

Identifiers & Regulatory

Product NDC 49483-697
Product ID 49483-697_2dc52443-77b2-5143-e063-6394a90a4958
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2022-02-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49483697
Hyphenated Format 49483-697

Supplemental Identifiers

RxCUI
198440
UPC
0349483697438
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 extra strength acetaminophen (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 400 TABLET in 1 BOTTLE (49483-697-43)
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2dc52443-77b2-5143-e063-6394a90a4958", "openfda": {"upc": ["0349483697438"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["c9f80d24-bd05-e1ce-e053-2995a90aa646"], "manufacturer_name": ["TIME CAP LABORATORIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "400 TABLET in 1 BOTTLE (49483-697-43)", "package_ndc": "49483-697-43", "marketing_start_date": "20220211"}], "brand_name": "EXTRA STRENGTH ACETAMINOPHEN", "product_id": "49483-697_2dc52443-77b2-5143-e063-6394a90a4958", "dosage_form": "TABLET", "product_ndc": "49483-697", "generic_name": "Acetaminophen", "labeler_name": "TIME CAP LABORATORIES, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EXTRA STRENGTH ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220211", "listing_expiration_date": "20261231"}