hydrocodone bitartrate and acetaminophen
Generic: hydrocodone bitartrate and acetaminophen
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
hydrocodone bitartrate and acetaminophen
Generic Name
hydrocodone bitartrate and acetaminophen
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET
Routes
Active Ingredients
acetaminophen 325 mg/1, hydrocodone bitartrate 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3447
Product ID
68071-3447_2d67b889-65d1-1c00-e063-6394a90a3d24
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210211
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2018-07-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713447
Hyphenated Format
68071-3447
Supplemental Identifiers
RxCUI
UPC
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
hydrocodone bitartrate and acetaminophen (source: ndc)
Generic Name
hydrocodone bitartrate and acetaminophen (source: ndc)
Application Number
ANDA210211 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 5 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (68071-3447-3)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d67b889-65d1-1c00-e063-6394a90a3d24", "openfda": {"upc": ["0368071344738"], "unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857002"], "spl_set_id": ["fed1eb12-3e39-1bf9-e053-6294a90afd77"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3447-3)", "package_ndc": "68071-3447-3", "marketing_start_date": "20230623"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "68071-3447_2d67b889-65d1-1c00-e063-6394a90a3d24", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68071-3447", "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": "5 mg/1"}], "application_number": "ANDA210211", "marketing_category": "ANDA", "marketing_start_date": "20180713", "listing_expiration_date": "20261231"}