heb
Generic: acetaminophen
Labeler: hebDrug Facts
Product Profile
Brand Name
heb
Generic Name
acetaminophen
Labeler
heb
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
acetaminophen 650 mg/1
Manufacturer
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
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 650 mg/1
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)
Packages (2)
Ingredients (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"}