acetaminophen

Generic: acetaminophen

Labeler: granules pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler granules pharmaceuticals inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-160
Product ID 70010-160_451b5125-968f-8c11-e063-6294a90a447c
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211544
Listing Expiration 2026-12-31
Marketing Start 2022-02-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70010160
Hyphenated Format 70010-160

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 acetaminophen (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
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-160-01)
source: ndc

Packages (1)

70010-160-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-160-01)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

ACETAMINOPHEN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "451b5125-968f-8c11-e063-6294a90a447c", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["d5352861-6926-f1b0-e053-2a95a90a7d66"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-160-01)", "package_ndc": "70010-160-01", "marketing_start_date": "20220215"}], "brand_name": "ACETAMINOPHEN", "product_id": "70010-160_451b5125-968f-8c11-e063-6294a90a447c", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "70010-160", "generic_name": "ACETAMINOPHEN", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_start_date": "20220215", "listing_expiration_date": "20261231"}