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NDC 50090-3878-01 Zolpidem Tartrate 10 mg/1 Details
Zolpidem Tartrate 10 mg/1
Zolpidem Tartrate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is ZOLPIDEM TARTRATE.
MedlinePlus Drug Summary
Zolpidem is used to treat insomnia (difficulty falling asleep or staying asleep). Zolpidem belongs to a class of medications called sedative-hypnotics. It works by slowing activity in the brain to allow sleep.
Related Packages: 50090-3878-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Zolpidem
Product Information
NDC | 50090-3878 |
---|---|
Product ID | 50090-3878_3e53970f-c97a-4d92-870b-feb3be6365f3 |
Associated GPIs | 60204080100315 |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Zolpidem Tartrate |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Zolpidem Tartrate |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 10 |
Active Ingredient Units | mg/1 |
Substance Name | ZOLPIDEM TARTRATE |
Labeler Name | A-S Medication Solutions |
Pharmaceutical Class | Central Nervous System Depression [PE], GABA A Agonists [MoA], Pyridines [CS], gamma-Aminobutyric Acid-ergic Agonist [EPC] |
DEA Schedule | CIV |
Marketing Category | ANDA |
Application Number | ANDA078413 |
Listing Certified Through | 2024-12-31 |
Package
NDC 50090-3878-01 (50090387801)
NDC Package Code | 50090-3878-1 |
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Billing NDC | 50090387801 |
Package | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3878-1) |
Marketing Start Date | 2018-11-28 |
NDC Exclude Flag | N |
Pricing Information | N/A |