Package 70010-160-01

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 70010-160-01
Digits Only 7001016001
Product NDC 70010-160
Product ID 70010-160_451b5125-968f-8c11-e063-6294a90a447c
Description

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

Marketing

Marketing Status
Marketed Since 2022-02-15
Brand acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

ACETAMINOPHEN ndc-match (0.95)

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"}