hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrocodone bitartrate and acetaminophen
Generic Name hydrocodone bitartrate and acetaminophen
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, hydrocodone bitartrate 7.5 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2645
Product ID 68071-2645_2a09ec53-48b8-1bf1-e063-6294a90a6e69
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
opioid agonist [epc] opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680712645
Hyphenated Format 68071-2645

Supplemental Identifiers

RxCUI
857005
UPC
0368071264531
UNII
362O9ITL9D NO70W886KK

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 7.5 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (68071-2645-2)
  • 30 TABLET in 1 BOTTLE (68071-2645-3)
source: ndc

Packages (2)

68071-2645-2 20 TABLET in 1 BOTTLE (68071-2645-2) 68071-2645-3 30 TABLET in 1 BOTTLE (68071-2645-3)

Ingredients (2)

acetaminophen (325 mg/1) hydrocodone bitartrate (7.5 mg/1)

Linked Drug Pages (1)

Hydrocodone Bitartrate and Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a09ec53-48b8-1bf1-e063-6294a90a6e69", "openfda": {"upc": ["0368071264531"], "unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857005"], "spl_set_id": ["d88e04c1-cd54-6a12-e053-2995a90a22b4"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-2645-2)", "package_ndc": "68071-2645-2", "marketing_start_date": "20240628"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-2645-3)", "package_ndc": "68071-2645-3", "marketing_start_date": "20220221"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "68071-2645_2a09ec53-48b8-1bf1-e063-6294a90a6e69", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68071-2645", "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": "7.5 mg/1"}], "application_number": "ANDA210211", "marketing_category": "ANDA", "marketing_start_date": "20180713", "listing_expiration_date": "20261231"}