Package 27808-130-01
Brand: hydrocodone bitartrate and acetaminophen
Generic: hydrocodone bitartrate and acetaminophenPackage Facts
Identity
Package NDC
27808-130-01
Digits Only
2780813001
Product NDC
27808-130
Description
473 mL in 1 BOTTLE, PLASTIC (27808-130-01)
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": "5b4bd464-17c3-42af-a519-ef795299e692", "openfda": {"upc": ["0327808130013"], "unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["1044427"], "spl_set_id": ["93b6dfdf-ba6e-4ea6-ab85-5ac121e33101"], "manufacturer_name": ["Cranbury Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (27808-130-01)", "package_ndc": "27808-130-01", "marketing_start_date": "20221230"}], "brand_name": "hydrocodone bitartrate and acetaminophen", "product_id": "27808-130_5b4bd464-17c3-42af-a519-ef795299e692", "dosage_form": "SOLUTION", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "27808-130", "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/15mL"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/15mL"}], "application_number": "ANDA201295", "marketing_category": "ANDA", "marketing_start_date": "20211230", "listing_expiration_date": "20271231"}