hydrocodone bitartrate and acetaminophen

Generic: hydrocodone bitartrate and acetaminophen

Labeler: a-s medication solutions
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 a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, hydrocodone bitartrate 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1778
Product ID 50090-1778_4eef7fec-90bb-4910-8ace-b3d3656c7273
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040409
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2000-10-20

Pharmacologic Class

Classes
opioid agonist [epc] opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500901778
Hyphenated Format 50090-1778

Supplemental Identifiers

RxCUI
857002
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 ANDA040409 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (50090-1778-0)
  • 12 TABLET in 1 BOTTLE (50090-1778-7)
source: ndc

Packages (2)

50090-1778-0 20 TABLET in 1 BOTTLE (50090-1778-0) 50090-1778-7 12 TABLET in 1 BOTTLE (50090-1778-7)

Ingredients (2)

acetaminophen (325 mg/1) hydrocodone bitartrate (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": "4eef7fec-90bb-4910-8ace-b3d3656c7273", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857002"], "spl_set_id": ["fc61200e-cc40-47c4-8792-c939c9877ae2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-1778-0)", "package_ndc": "50090-1778-0", "marketing_start_date": "20150414"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE (50090-1778-7)", "package_ndc": "50090-1778-7", "marketing_start_date": "20190129"}], "brand_name": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN", "product_id": "50090-1778_4eef7fec-90bb-4910-8ace-b3d3656c7273", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "50090-1778", "dea_schedule": "CII", "generic_name": "HYDROCODONE BITARTRATE AND ACETAMINOPHEN", "labeler_name": "A-S Medication Solutions", "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": "ANDA040409", "marketing_category": "ANDA", "marketing_start_date": "20001020", "listing_expiration_date": "20271231"}