hydrocodone bitartrate and acetaminophen (72162-2271)

Drug Facts

Product Profile

Brand Name hydrocodone bitartrate and acetaminophen

Generic Name hydrocodone bitartrate and acetaminophen

Labeler bryant ranch prepack

Dosage Form TABLET

Routes

ORAL

Active Ingredients

acetaminophen 325 mg/1, hydrocodone bitartrate 10 mg/1

Manufacturer

Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2271

Product ID 72162-2271_29491adb-d95d-4f68-ac01-61bad73e08fc

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA202991

DEA Schedule cii

Listing Expiration 2026-12-31

Marketing Start 2016-04-12

Pharmacologic Class

Classes

opioid agonist [epc] opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622271

Hyphenated Format 72162-2271

Supplemental Identifiers

RxCUI

856999

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 ANDA202991 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

325 mg/1
10 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (72162-2271-1)
500 TABLET in 1 BOTTLE (72162-2271-5)

source: ndc

Packages (2)

72162-2271-1 100 TABLET in 1 BOTTLE (72162-2271-1) 72162-2271-5 500 TABLET in 1 BOTTLE (72162-2271-5)

Ingredients (2)

acetaminophen (325 mg/1) hydrocodone bitartrate (10 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": "29491adb-d95d-4f68-ac01-61bad73e08fc", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856999"], "spl_set_id": ["29491adb-d95d-4f68-ac01-61bad73e08fc"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2271-1)", "package_ndc": "72162-2271-1", "marketing_start_date": "20160412"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-2271-5)", "package_ndc": "72162-2271-5", "marketing_start_date": "20160412"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "72162-2271_29491adb-d95d-4f68-ac01-61bad73e08fc", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "72162-2271", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "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": "ANDA202991", "marketing_category": "ANDA", "marketing_start_date": "20160412", "listing_expiration_date": "20261231"}