zolpidem tartrate
Generic: zolpidem tartrate
Labeler: directrxDrug Facts
Product Profile
Brand Name
zolpidem tartrate
Generic Name
zolpidem tartrate
Labeler
directrx
Dosage Form
TABLET
Routes
Active Ingredients
zolpidem tartrate 10 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
61919663
Hyphenated Format
61919-663
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (61919-663-30)
- 60 TABLET in 1 BOTTLE (61919-663-60)
Packages (2)
Ingredients (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"}