pain relief extra strength

Generic: acetaminophen

Labeler: topco associates llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief extra strength
Generic Name acetaminophen
Labeler topco associates llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
TopCo Associates LLC

Identifiers & Regulatory

Product NDC 36800-905
Product ID 36800-905_2850a74e-12a4-88d3-e063-6394a90a831b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2011-08-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 36800905
Hyphenated Format 36800-905

Supplemental Identifiers

RxCUI
198440
UPC
0036800128309
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 pain relief extra strength (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
  • 1 BOTTLE, PLASTIC in 1 CARTON (36800-905-02) / 60 TABLET in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (36800-905-04) / 100 TABLET in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

36800-905-02 1 BOTTLE, PLASTIC in 1 CARTON (36800-905-02) / 60 TABLET in 1 BOTTLE, PLASTIC 36800-905-04 1 BOTTLE, PLASTIC in 1 CARTON (36800-905-04) / 100 TABLET in 1 BOTTLE, PLASTIC

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Pain Relief Extra Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2850a74e-12a4-88d3-e063-6394a90a831b", "openfda": {"upc": ["0036800128309"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["bdb01b3e-ad34-4003-9b9a-e83a2c0e90bb"], "manufacturer_name": ["TopCo Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (36800-905-02)  / 60 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "36800-905-02", "marketing_start_date": "20110830"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (36800-905-04)  / 100 TABLET in 1 BOTTLE, PLASTIC", "package_ndc": "36800-905-04", "marketing_start_date": "20110830"}], "brand_name": "Pain Relief Extra Strength", "product_id": "36800-905_2850a74e-12a4-88d3-e063-6394a90a831b", "dosage_form": "TABLET", "product_ndc": "36800-905", "generic_name": "Acetaminophen", "labeler_name": "TopCo Associates LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110830", "listing_expiration_date": "20261231"}