zolpidem tartrate

Generic: zolpidem tartrate

Labeler: directrx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zolpidem tartrate
Generic Name zolpidem tartrate
Labeler directrx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

zolpidem tartrate 10 mg/1

Manufacturer
DirectRX

Identifiers & Regulatory

Product NDC 61919-663
Product ID 61919-663_1bcf8ea2-de5f-2078-e063-6394a90a9bb6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077903
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2015-12-02

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 61919663
Hyphenated Format 61919-663

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 ANDA077903 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (61919-663-30)
  • 60 TABLET in 1 BOTTLE (61919-663-60)
source: ndc

Packages (2)

Ingredients (1)

zolpidem tartrate (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1bcf8ea2-de5f-2078-e063-6394a90a9bb6", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["25f1176d-5195-1a99-e054-00144ff8d46c"], "manufacturer_name": ["DirectRX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (61919-663-30)", "package_ndc": "61919-663-30", "marketing_start_date": "20151202"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (61919-663-60)", "package_ndc": "61919-663-60", "marketing_start_date": "20151202"}], "brand_name": "ZOLPIDEM TARTRATE", "product_id": "61919-663_1bcf8ea2-de5f-2078-e063-6394a90a9bb6", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "61919-663", "dea_schedule": "CIV", "generic_name": "ZOLPIDEM TARTRATE", "labeler_name": "DirectRX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZOLPIDEM TARTRATE", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA077903", "marketing_category": "ANDA", "marketing_start_date": "20151202", "listing_expiration_date": "20261231"}