Package 37835-512-01

Brand: acetaminophen

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 37835-512-01
Digits Only 3783551201
Product NDC 37835-512
Product ID 37835-512_30d44923-02f8-c4ea-e063-6294a90a935a
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (37835-512-01)

Marketing

Marketing Status
Marketed Since 2025-03-01
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": "30d44923-02f8-c4ea-e063-6294a90a935a", "openfda": {"unii": ["362O9ITL9D"], "rxcui": ["1148399"], "spl_set_id": ["ab2f0834-bdef-4862-b549-5a8161f8420b"], "manufacturer_name": ["Bi-Mart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (37835-512-01)", "package_ndc": "37835-512-01", "marketing_start_date": "20250301"}], "brand_name": "ACETAMINOPHEN", "product_id": "37835-512_30d44923-02f8-c4ea-e063-6294a90a935a", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "37835-512", "generic_name": "ACETAMINOPHEN", "labeler_name": "Bi-Mart", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}], "application_number": "ANDA211544", "marketing_category": "ANDA", "marketing_start_date": "20190418", "listing_expiration_date": "20261231"}