Package 0603-2540-21

Brand: butalbital and acetaminophen

Generic: butalbital and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 0603-2540-21
Digits Only 0603254021
Product NDC 0603-2540
Description

100 TABLET in 1 BOTTLE (0603-2540-21)

Marketing

Marketing Status
Marketed Since 1999-06-03
Brand butalbital and acetaminophen
Generic butalbital and acetaminophen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d7cd016-87b7-12bf-e063-6294a90ac288", "openfda": {"nui": ["N0000175693", "M0002177"], "unii": ["362O9ITL9D", "KHS0AZ4JVK"], "rxcui": ["197426"], "spl_set_id": ["e619b656-4123-4878-b601-b0edad3c428b"], "pharm_class_cs": ["Barbiturates [CS]"], "pharm_class_epc": ["Barbiturate [EPC]"], "manufacturer_name": ["Endo USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0603-2540-21)", "package_ndc": "0603-2540-21", "marketing_start_date": "19990603"}], "brand_name": "butalbital and acetaminophen", "product_id": "0603-2540_2d7cd016-87b7-12bf-e063-6294a90ac288", "dosage_form": "TABLET", "pharm_class": ["Barbiturate [EPC]", "Barbiturates [CS]"], "product_ndc": "0603-2540", "generic_name": "butalbital and acetaminophen", "labeler_name": "Endo USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "butalbital and acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "BUTALBITAL", "strength": "50 mg/1"}], "application_number": "ANDA089987", "marketing_category": "ANDA", "marketing_start_date": "19990603", "listing_expiration_date": "20261231"}