pain relief extra strength, non-aspirin

Generic: acetaminophen

Labeler: chain drug marketing association inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief extra strength, non-aspirin
Generic Name acetaminophen
Labeler chain drug marketing association inc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION INC

Identifiers & Regulatory

Product NDC 63868-987
Product ID 63868-987_827f97ea-efba-4fe6-a603-aaea8cdcd902
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Marketing Start 2004-05-10
Marketing End 2028-04-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63868987
Hyphenated Format 63868-987

Supplemental Identifiers

RxCUI
198440
UPC
0635515956094
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, non-aspirin (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 (63868-987-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (63868-987-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (2)

Ingredients (1)

acetaminophen (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "827f97ea-efba-4fe6-a603-aaea8cdcd902", "openfda": {"upc": ["0635515956094"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["1fb5e871-45fd-46fe-bf73-5192f8316e8e"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-987-10)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-987-10", "marketing_end_date": "20280430", "marketing_start_date": "20040510"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-987-50)  / 50 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "63868-987-50", "marketing_end_date": "20280430", "marketing_start_date": "20040510"}], "brand_name": "Pain Relief Extra Strength, Non-Aspirin", "product_id": "63868-987_827f97ea-efba-4fe6-a603-aaea8cdcd902", "dosage_form": "TABLET, COATED", "product_ndc": "63868-987", "generic_name": "Acetaminophen", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Extra Strength, Non-Aspirin", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20280430", "marketing_start_date": "20040510"}