Package 0121-2316-50
Brand: hydrocodone bitartrate and acetaminophen
Generic: hydrocodone bitartrate and acetaminophenPackage Facts
Identity
Package NDC
0121-2316-50
Digits Only
0121231650
Product NDC
0121-2316
Description
5 TRAY in 1 CASE (0121-2316-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE
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": "1c5f2752-d5b9-4830-bc53-31c816f2bc09", "openfda": {"unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856940"], "spl_set_id": ["c29b97e9-8097-4d87-a420-ccf5aec8274a"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 TRAY in 1 CASE (0121-2316-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE", "package_ndc": "0121-2316-50", "marketing_start_date": "20200521"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "0121-2316_1c5f2752-d5b9-4830-bc53-31c816f2bc09", "dosage_form": "SOLUTION", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "0121-2316", "dea_schedule": "CII", "generic_name": "HYDROCODONE BITARTRATE and ACETAMINOPHEN", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/15mL"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/15mL"}], "application_number": "ANDA040838", "marketing_category": "ANDA", "marketing_start_date": "20130729", "listing_expiration_date": "20271231"}