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 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2649
Product ID 50090-2649_b75ac94e-cbd4-40de-97df-db9eeae46947
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078413
DEA Schedule civ
Listing Expiration 2027-12-31
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 500902649
Hyphenated Format 50090-2649

Supplemental Identifiers

RxCUI
854876
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
  • 5 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-2649-0)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-2649-1)
  • 3 TABLET, FILM COATED in 1 BOTTLE (50090-2649-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-2649-4)
source: ndc

Packages (4)

50090-2649-0 20 TABLET, FILM COATED in 1 BOTTLE (50090-2649-0) 50090-2649-1 30 TABLET, FILM COATED in 1 BOTTLE (50090-2649-1) 50090-2649-3 3 TABLET, FILM COATED in 1 BOTTLE (50090-2649-3) 50090-2649-4 60 TABLET, FILM COATED in 1 BOTTLE (50090-2649-4)

Ingredients (1)

zolpidem tartrate (5 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": "b75ac94e-cbd4-40de-97df-db9eeae46947", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854876"], "spl_set_id": ["f67ef513-1b2c-42fe-bf33-4c7e9db191a3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-2649-0)", "package_ndc": "50090-2649-0", "marketing_start_date": "20161220"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-2649-1)", "package_ndc": "50090-2649-1", "marketing_start_date": "20170117"}, {"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (50090-2649-3)", "package_ndc": "50090-2649-3", "marketing_start_date": "20161128"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-2649-4)", "package_ndc": "50090-2649-4", "marketing_start_date": "20241115"}], "brand_name": "Zolpidem Tartrate", "product_id": "50090-2649_b75ac94e-cbd4-40de-97df-db9eeae46947", "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": "50090-2649", "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": "5 mg/1"}], "application_number": "ANDA078413", "marketing_category": "ANDA", "marketing_start_date": "20070504", "listing_expiration_date": "20271231"}