zolpidem tartrate

Generic: zolpidem tartrate

Labeler: golden state medical supply, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zolpidem tartrate
Generic Name zolpidem tartrate
Labeler golden state medical supply, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

zolpidem tartrate 10 mg/1

Manufacturer
Golden State Medical Supply, Inc.

Identifiers & Regulatory

Product NDC 51407-942
Product ID 51407-942_2b5cd5f8-4872-d3e1-e063-6394a90aca8d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077214
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2007-04-23

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 51407942
Hyphenated Format 51407-942

Supplemental Identifiers

RxCUI
854873 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 ANDA077214 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (51407-942-01)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (51407-942-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (51407-942-30)
source: ndc

Packages (3)

51407-942-01 100 TABLET, FILM COATED in 1 BOTTLE (51407-942-01) 51407-942-10 1000 TABLET, FILM COATED in 1 BOTTLE (51407-942-10) 51407-942-30 30 TABLET, FILM COATED in 1 BOTTLE (51407-942-30)

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": "2b5cd5f8-4872-d3e1-e063-6394a90aca8d", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873", "854876"], "spl_set_id": ["2b5cf535-ccdc-ecd7-e063-6394a90a726e"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (51407-942-01)", "package_ndc": "51407-942-01", "marketing_start_date": "20241206"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (51407-942-10)", "package_ndc": "51407-942-10", "marketing_start_date": "20241206"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51407-942-30)", "package_ndc": "51407-942-30", "marketing_start_date": "20241206"}], "brand_name": "ZOLPIDEM TARTRATE", "product_id": "51407-942_2b5cd5f8-4872-d3e1-e063-6394a90aca8d", "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": "51407-942", "dea_schedule": "CIV", "generic_name": "zolpidem tartrate", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZOLPIDEM TARTRATE", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA077214", "marketing_category": "ANDA", "marketing_start_date": "20070423", "listing_expiration_date": "20261231"}