Package 71205-314-08

Brand: medi-first non-aspirin extra strength

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 71205-314-08
Digits Only 7120531408
Product NDC 71205-314
Description

8 TABLET, FILM COATED in 1 PACKET (71205-314-08)

Marketing

Marketing Status
Marketed Since 2020-02-05
Brand medi-first non-aspirin extra strength
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9608b190-4f25-48f2-a49c-11c360656608", "openfda": {"upc": ["0371205314040"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["9071b047-5463-4f65-b775-bfb0ce066527"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 PACKET (71205-314-04)", "package_ndc": "71205-314-04", "marketing_start_date": "20190901"}, {"sample": false, "description": "8 TABLET, FILM COATED in 1 PACKET (71205-314-08)", "package_ndc": "71205-314-08", "marketing_start_date": "20200205"}], "brand_name": "MEDI-FIRST Non-Aspirin Extra Strength", "product_id": "71205-314_9608b190-4f25-48f2-a49c-11c360656608", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71205-314", "generic_name": "Acetaminophen", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MEDI-FIRST Non-Aspirin Extra Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20081230", "listing_expiration_date": "20261231"}