Package 10135-829-01

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 10135-829-01
Digits Only 1013582901
Product NDC 10135-829
Product ID 10135-829_4a183bb4-ec85-c7d2-e063-6394a90ad356
Description

100 TABLET in 1 BOTTLE (10135-829-01)

Marketing

Marketing Status
Marketed Since 2026-02-01
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": "4a183bb4-ec85-c7d2-e063-6394a90ad356", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["198440"], "spl_set_id": ["4a183b7d-3a1e-5557-e063-6294a90a5493"], "manufacturer_name": ["Marlex Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10135-829-01)", "package_ndc": "10135-829-01", "marketing_start_date": "20260201"}], "brand_name": "Acetaminophen", "product_id": "10135-829_4a183bb4-ec85-c7d2-e063-6394a90ad356", "dosage_form": "TABLET", "product_ndc": "10135-829", "generic_name": "Acetaminophen", "labeler_name": "Marlex Pharmaceuticals 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": "20260201", "listing_expiration_date": "20271231"}