zolpidem tartrate

Generic: zolpidem tartrate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zolpidem tartrate
Generic Name zolpidem tartrate
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

zolpidem tartrate 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3878
Product ID 50090-3878_f0422eb4-b8c1-410e-9a32-4538f743ff92
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078413
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2007-05-04

Pharmacologic Class

Classes
central nervous system depression [pe] gaba a receptor positive modulators [moa] gamma-aminobutyric acid a receptor positive modulator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500903878
Hyphenated Format 50090-3878

Supplemental Identifiers

RxCUI
854873
UNII
WY6W63843K

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 zolpidem tartrate (source: ndc)
Generic Name zolpidem tartrate (source: ndc)
Application Number ANDA078413 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE (50090-3878-0)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-3878-1)
source: ndc

Packages (2)

50090-3878-0 10 TABLET, FILM COATED in 1 BOTTLE (50090-3878-0) 50090-3878-1 30 TABLET, FILM COATED in 1 BOTTLE (50090-3878-1)

Ingredients (1)

zolpidem tartrate (10 mg/1)

Linked Drug Pages (1)

Zolpidem Tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f0422eb4-b8c1-410e-9a32-4538f743ff92", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["ef72eb73-d058-4ca3-9013-691aae8426fb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-3878-0)", "package_ndc": "50090-3878-0", "marketing_start_date": "20181128"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-3878-1)", "package_ndc": "50090-3878-1", "marketing_start_date": "20181128"}], "brand_name": "Zolpidem Tartrate", "product_id": "50090-3878_f0422eb4-b8c1-410e-9a32-4538f743ff92", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "50090-3878", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolpidem Tartrate", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA078413", "marketing_category": "ANDA", "marketing_start_date": "20070504", "listing_expiration_date": "20261231"}