zolpidem tartrate

Generic: zolpidem tartrate

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zolpidem tartrate
Generic Name zolpidem tartrate
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

zolpidem tartrate 10 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-0074
Product ID 0093-0074_6d1230f8-c080-4fc7-a9ef-72a4a40c69ff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076410
DEA Schedule civ
Marketing Start 2007-04-23
Marketing End 2026-04-30

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 00930074
Hyphenated Format 0093-0074

Supplemental Identifiers

RxCUI
854873 854876
UPC
0300930074011
UNII
WY6W63843K

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 zolpidem tartrate (source: ndc)
Generic Name zolpidem tartrate (source: ndc)
Application Number ANDA076410 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0093-0074-01)
source: ndc

Packages (1)

0093-0074-01 100 TABLET, FILM COATED in 1 BOTTLE (0093-0074-01)

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": "6d1230f8-c080-4fc7-a9ef-72a4a40c69ff", "openfda": {"upc": ["0300930074011"], "unii": ["WY6W63843K"], "rxcui": ["854873", "854876"], "spl_set_id": ["c784cf9d-de8f-44b6-b52f-a0e7c0d35e48"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-0074-01)", "package_ndc": "0093-0074-01", "marketing_end_date": "20260430", "marketing_start_date": "20070423"}], "brand_name": "Zolpidem Tartrate", "product_id": "0093-0074_6d1230f8-c080-4fc7-a9ef-72a4a40c69ff", "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": "0093-0074", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolpidem Tartrate", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA076410", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20070423"}