Package 66267-319-30

Brand: hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 66267-319-30
Digits Only 6626731930
Product NDC 66267-319
Description

30 TABLET in 1 BOTTLE (66267-319-30)

Marketing

Marketing Status
Marketed Since 2019-06-11
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": "1fa6a518-e720-2232-e063-6294a90a73e4", "openfda": {"upc": ["0366267319300"], "unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856999"], "spl_set_id": ["8b132cf3-c138-59ae-e053-2995a90a98a2"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (66267-319-30)", "package_ndc": "66267-319-30", "marketing_start_date": "20190611"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "66267-319_1fa6a518-e720-2232-e063-6294a90a73e4", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "66267-319", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA201013", "marketing_category": "ANDA", "marketing_start_date": "20120411", "listing_expiration_date": "20261231"}