Package 68047-721-01
Brand: butalbital and acetaminophen
Generic: butalbital and acetaminophenPackage Facts
Identity
Package NDC
68047-721-01
Digits Only
6804772101
Product NDC
68047-721
Description
100 TABLET in 1 BOTTLE (68047-721-01)
Marketing
Marketing Status
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": "41348343-4fef-7234-e063-6394a90af41d", "openfda": {"nui": ["N0000175693", "M0002177"], "upc": ["0368047753014", "0368047752017", "0368047721013"], "unii": ["KHS0AZ4JVK", "362O9ITL9D"], "rxcui": ["197426", "1724446", "2279007"], "spl_set_id": ["326c83fc-afed-45ad-9c87-f47968fa1d2a"], "pharm_class_cs": ["Barbiturates [CS]"], "pharm_class_epc": ["Barbiturate [EPC]"], "manufacturer_name": ["Larken Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68047-721-01)", "package_ndc": "68047-721-01", "marketing_start_date": "20151204"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68047-721-30)", "package_ndc": "68047-721-30", "marketing_start_date": "20151204"}], "brand_name": "Butalbital And Acetaminophen", "product_id": "68047-721_41348343-4fef-7234-e063-6394a90af41d", "dosage_form": "TABLET", "pharm_class": ["Barbiturate [EPC]", "Barbiturates [CS]"], "product_ndc": "68047-721", "dea_schedule": "CIII", "generic_name": "butalbital and acetaminophen", "labeler_name": "Larken Laboratories, Inc.", "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": "ANDA203484", "marketing_category": "ANDA", "marketing_start_date": "20151204", "listing_expiration_date": "20261231"}