oxycodone and acetaminophen (71930-046)

Drug Facts

Product Profile

Brand Name oxycodone and acetaminophen

Generic Name oxycodone and acetaminophen

Labeler eywa pharma inc

Dosage Form TABLET

Routes

ORAL

Active Ingredients

acetaminophen 325 mg/1, oxycodone hydrochloride 7.5 mg/1

Manufacturer

Eywa Pharma Inc

Identifiers & Regulatory

Product NDC 71930-046

Product ID 71930-046_3dba33c1-5d2b-49d4-becb-345947236687

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA207510

DEA Schedule cii

Listing Expiration 2026-12-31

Marketing Start 2019-06-01

Pharmacologic Class

Classes

full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71930046

Hyphenated Format 71930-046

Supplemental Identifiers

RxCUI

1049214 1049221 1049225

UPC

0371930045127 0371930046124 0371930047121

UNII

C1ENJ2TE6C 362O9ITL9D

Packaging Origin

Original Packager

true

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 oxycodone and acetaminophen (source: ndc)

Generic Name oxycodone and acetaminophen (source: ndc)

Application Number ANDA207510 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

325 mg/1
7.5 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (71930-046-12)
500 TABLET in 1 BOTTLE (71930-046-52)

source: ndc

Packages (2)

71930-046-12 100 TABLET in 1 BOTTLE (71930-046-12) 71930-046-52 500 TABLET in 1 BOTTLE (71930-046-52)

Ingredients (2)

acetaminophen (325 mg/1) oxycodone hydrochloride (7.5 mg/1)

Linked Drug Pages (1)

OXYCODONE AND ACETAMINOPHEN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "3dba33c1-5d2b-49d4-becb-345947236687", "openfda": {"upc": ["0371930045127", "0371930046124", "0371930047121"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225"], "spl_set_id": ["1da85ac1-46a2-4081-b533-4890ec9e0482"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71930-046-12)", "package_ndc": "71930-046-12", "marketing_start_date": "20190601"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71930-046-52)", "package_ndc": "71930-046-52", "marketing_start_date": "20190601"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "71930-046_3dba33c1-5d2b-49d4-becb-345947236687", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71930-046", "dea_schedule": "CII", "generic_name": "oxycodone and acetaminophen", "labeler_name": "Eywa Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE AND ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA207510", "marketing_category": "ANDA", "marketing_start_date": "20190601", "listing_expiration_date": "20261231"}