Package 70677-1242-1

Brand: extra strength pain releif

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 70677-1242-1
Digits Only 7067712421
Product NDC 70677-1242
Description

120 TABLET, FILM COATED in 1 BOTTLE (70677-1242-1)

Marketing

Marketing Status
Marketed Since 2024-02-02
Brand extra strength pain releif
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "498af382-ead9-9b5d-e063-6294a90a7852", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["0392db17-c4f3-424b-9dee-549fc5df61c5"], "manufacturer_name": ["Strategic Sourcing Services, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (70677-1242-1)", "package_ndc": "70677-1242-1", "marketing_start_date": "20240202"}], "brand_name": "EXTRA STRENGTH PAIN RELEIF", "product_id": "70677-1242_498af382-ead9-9b5d-e063-6294a90a7852", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70677-1242", "generic_name": "ACETAMINOPHEN", "labeler_name": "Strategic Sourcing Services, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EXTRA STRENGTH PAIN RELEIF", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240202", "listing_expiration_date": "20271231"}