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United States · US · US:63629-3549_0e3b2506-9d0e-40cf-b8b1-72d0ef4a0c37
ZOLPIDEM TARTRATE
Orange BookUNIISPLATC N05CF02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN05CF02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 10
- ndc11636293549025 TABLET in 1 BOTTLE (63629-3549-0)
- ndc11636293549130 TABLET in 1 BOTTLE (63629-3549-1)
- ndc11636293549260 TABLET in 1 BOTTLE (63629-3549-2)
- ndc11636293549310 TABLET in 1 BOTTLE (63629-3549-3)
- ndc116362935494100 TABLET in 1 BOTTLE (63629-3549-4)
- ndc11636293549520 TABLET in 1 BOTTLE (63629-3549-5)
- ndc11636293549690 TABLET in 1 BOTTLE (63629-3549-6)
- ndc11636293549756 TABLET in 1 BOTTLE (63629-3549-7)
- ndc11636293549828 TABLET in 1 BOTTLE (63629-3549-8)
- ndc116362935499120 TABLET in 1 BOTTLE (63629-3549-9)
Annotations
UNII (FDA Substance ID)
WY6W63843K
ZOLPIDEM TARTRATE
RxCUI 221183
Orange Book
A077903
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "WY6W63843K",
"rxcui": "221183",
"inchikey": "VXRDAMSNTXUHFX-CEAXSRTFSA-N",
"display_name": "ZOLPIDEM TARTRATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"b49f6c18-e155-4728-a79a-9354e8c3c8f4": {
"match": "brand_token",
"title": "ZOLPIDEM TARTRATE CAPSULE [UMEDICA LABORATORIES USA INC.]",
"spl_version": "2",
"published_date": "2026-05-27"
}
},
"productid": "63629-3549_0e3b2506-9d0e-40cf-b8b1-72d0ef4a0c37",
"productndc": "63629-3549",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "077903",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "001",
"approval_date": "Aug 17, 2007"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "002",
"approval_date": "Aug 17, 2007"
}
],
"appl_type": "A"
},
"dea_schedule": "CIV",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "ZOLPIDEM TARTRATE",
"proprietary_name": "ZOLPIDEM TARTRATE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA077903",
"marketing_category": "ANDA",
"nonproprietary_name": "zolpidem tartrate",
"start_marketing_date": "20070905",
"active_numerator_strength": "5"
}Related drugs
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