8hr pain relief

Generic: acetaminophen

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name 8hr pain relief
Generic Name acetaminophen
Labeler target corporation
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-928
Product ID 11673-928_13ae3e9d-92cc-3471-e063-6394a90acbfb
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA215486
Listing Expiration 2026-12-31
Marketing Start 2022-11-07

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673928
Hyphenated Format 11673-928

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 8hr pain relief (source: ndc)
Generic Name acetaminophen (source: ndc)
Application Number ANDA215486 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (11673-928-01) / 100 TABLET, 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": "13ae3e9d-92cc-3471-e063-6394a90acbfb", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["e8b48f37-6023-ba04-e053-2a95a90a0e6c"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-928-01)  / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "11673-928-01", "marketing_start_date": "20221130"}], "brand_name": "8HR Pain Relief", "product_id": "11673-928_13ae3e9d-92cc-3471-e063-6394a90acbfb", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "11673-928", "generic_name": "Acetaminophen", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "8HR Pain Relief", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA215486", "marketing_category": "ANDA", "marketing_start_date": "20221107", "listing_expiration_date": "20261231"}