Package 69842-635-07

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 69842-635-07
Digits Only 6984263507
Product NDC 69842-635
Description

1 BOTTLE in 1 CARTON (69842-635-07) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-10-13
Brand acetaminophen
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8394aaec-e897-48bb-bda2-cc2b64a6cd64", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["e577fdf0-85b1-1471-e053-2995a90a6fcd"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-635-07)  / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "69842-635-07", "marketing_start_date": "20221013"}], "brand_name": "Acetaminophen", "product_id": "69842-635_8394aaec-e897-48bb-bda2-cc2b64a6cd64", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "69842-635", "generic_name": "Acetaminophen", "labeler_name": "CVS Pharmacy, Inc.", "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": "20221013", "listing_expiration_date": "20261231"}