Package 27808-114-02
Brand: hydrocodone bitartrate and acetaminophen
Generic: hydrocodone bitartrate and acetaminophenPackage Facts
Identity
Package NDC
27808-114-02
Digits Only
2780811402
Product NDC
27808-114
Description
500 TABLET in 1 BOTTLE (27808-114-02)
Marketing
Marketing Status
Brand
hydrocodone bitartrate and acetaminophen
Generic
hydrocodone bitartrate and acetaminophen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b87bebc7-651b-4b88-8921-cfddb4265559", "openfda": {"upc": ["0327808115010", "0327808114013", "0327808116017"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856980", "856987", "856992"], "spl_set_id": ["d8fe4ae4-bd19-42eb-b74d-f302b3f914ee"], "manufacturer_name": ["Cranbury Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (27808-114-01)", "package_ndc": "27808-114-01", "marketing_start_date": "20160407"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (27808-114-02)", "package_ndc": "27808-114-02", "marketing_start_date": "20160407"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "27808-114_b87bebc7-651b-4b88-8921-cfddb4265559", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "27808-114", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Cranbury Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA202214", "marketing_category": "ANDA", "marketing_start_date": "20160407", "listing_expiration_date": "20261231"}