heb

Generic: acetaminophen

Labeler: heb
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

acetaminophen 650 mg/1

Manufacturer
HEB

Identifiers & Regulatory

Product NDC 37808-120
Product ID 37808-120_f924d0ab-cfa6-7dbe-e053-6394a90abc40
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA211544
Listing Expiration 2026-12-31
Marketing Start 2020-03-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808120
Hyphenated Format 37808-120

Supplemental Identifiers

RxCUI
1148399
UPC
0041220221707
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 heb (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 (37808-120-02) / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (37808-120-04)
source: ndc

Packages (2)

Ingredients (1)

acetaminophen (650 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f924d0ab-cfa6-7dbe-e053-6394a90abc40", "openfda": {"upc": ["0041220221707"], "unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["96b1808f-defa-28cb-e053-2995a90a563b"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (37808-120-02)  / 50 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC", "package_ndc": "37808-120-02", "marketing_start_date": "20200801"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (37808-120-04)", "package_ndc": "37808-120-04", "marketing_start_date": "20200301"}], "brand_name": "HEB", "product_id": "37808-120_f924d0ab-cfa6-7dbe-e053-6394a90abc40", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "37808-120", "generic_name": "Acetaminophen", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HEB", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}