Package 71399-1026-1

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 71399-1026-1
Digits Only 7139910261
Product NDC 71399-1026
Description

100 TABLET in 1 BOTTLE (71399-1026-1)

Marketing

Marketing Status
Marketed Since 2024-12-06
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": "48c2f5ad-4a7a-462b-e063-6294a90ab90a", "openfda": {"upc": ["0371399102614", "0371399102621"], "unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["ab79fd60-8315-4c63-8045-1b0511ac268f"], "manufacturer_name": ["Akron Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71399-1026-1)", "package_ndc": "71399-1026-1", "marketing_start_date": "20241206"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71399-1026-2)", "package_ndc": "71399-1026-2", "marketing_start_date": "20241206"}], "brand_name": "ACETAMINOPHEN", "product_id": "71399-1026_48c2f5ad-4a7a-462b-e063-6294a90ab90a", "dosage_form": "TABLET", "product_ndc": "71399-1026", "generic_name": "Acetaminophen", "labeler_name": "Akron Pharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241206", "listing_expiration_date": "20271231"}