acetaminophen

Generic: acetaminophen

Labeler: kroger company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name acetaminophen
Generic Name acetaminophen
Labeler kroger company
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1

Manufacturer
KROGER COMPANY

Identifiers & Regulatory

Product NDC 30142-157
Product ID 30142-157_5cd5f635-7f27-4b34-bb0b-779d36c25398
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207229
Listing Expiration 2026-12-31
Marketing Start 2021-05-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 30142157
Hyphenated Format 30142-157

Supplemental Identifiers

RxCUI
1148399
UPC
0041260016325
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 ANDA207229 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (30142-157-07) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE
  • 225 TABLET, EXTENDED RELEASE in 1 BOTTLE (30142-157-35)
source: ndc

Packages (2)

30142-157-07 1 BOTTLE in 1 CARTON (30142-157-07) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE 30142-157-35 225 TABLET, EXTENDED RELEASE in 1 BOTTLE (30142-157-35)

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": "5cd5f635-7f27-4b34-bb0b-779d36c25398", "openfda": {"upc": ["0041260016325"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["b9b63c38-83e7-62d2-e053-2a95a90a5526"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (30142-157-07)  / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "30142-157-07", "marketing_start_date": "20210525"}, {"sample": false, "description": "225 TABLET, EXTENDED RELEASE in 1 BOTTLE (30142-157-35)", "package_ndc": "30142-157-35", "marketing_start_date": "20210525"}], "brand_name": "Acetaminophen", "product_id": "30142-157_5cd5f635-7f27-4b34-bb0b-779d36c25398", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "30142-157", "generic_name": "Acetaminophen", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA207229", "marketing_category": "ANDA", "marketing_start_date": "20210525", "listing_expiration_date": "20261231"}