8 hour pain relief

Generic: acetaminophen

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

Drug Facts

Product Profile

Brand Name 8 hour pain relief
Generic Name acetaminophen
Labeler chain drug marketing association inc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION INC

Identifiers & Regulatory

Product NDC 63868-679
Product ID 63868-679_24357a94-9aa7-4606-e063-6294a90ad492
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211544
Marketing Start 2020-08-01
Marketing End 2027-01-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63868679
Hyphenated Format 63868-679

Supplemental Identifiers

RxCUI
1148399
UPC
0635515958593
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 8 hour pain relief (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA211544 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (63868-679-50) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24357a94-9aa7-4606-e063-6294a90ad492", "openfda": {"upc": ["0635515958593"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["1da0bd23-9f26-4913-9ebf-1fd8b0fb3bd3"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (63868-679-50)  / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "63868-679-50", "marketing_end_date": "20270131", "marketing_start_date": "20200801"}], "brand_name": "8 Hour Pain Relief", "product_id": "63868-679_24357a94-9aa7-4606-e063-6294a90ad492", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "63868-679", "generic_name": "Acetaminophen", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "8 Hour Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_end_date": "20270131", "marketing_start_date": "20200801"}