pain relief 8 hr

Generic: acetaminophen

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief 8 hr
Generic Name acetaminophen
Labeler h e b
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-747
Product ID 37808-747_6b75a346-403e-45e1-a74d-21c0b8dcd8ed
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA075077
Listing Expiration 2026-12-31
Marketing Start 2017-02-24

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808747
Hyphenated Format 37808-747

Supplemental Identifiers

RxCUI
1148399
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 8 hr (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA075077 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (37808-747-71) / 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
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": "6b75a346-403e-45e1-a74d-21c0b8dcd8ed", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["b5c7e93b-e626-49c3-a7d4-773475f945ae"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-747-71)  / 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "37808-747-71", "marketing_start_date": "20170224"}], "brand_name": "Pain Relief 8 HR", "product_id": "37808-747_6b75a346-403e-45e1-a74d-21c0b8dcd8ed", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "37808-747", "generic_name": "Acetaminophen", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief 8 HR", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA075077", "marketing_category": "ANDA", "marketing_start_date": "20170224", "listing_expiration_date": "20261231"}