FDA.reportPublic FDA data

NDC 68180-779-11 - ZOLPIDEM TARTRATE

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
68180-779
Requested NDC
68180-779-11
Package NDCs from labels
68180-779-06, 68180-779-02, 68180-779-03, 68180-779-11, 68180-779-04, 68180-779-01
Manufacturer
Bryant Ranch Prepack
Effective date
2026-07-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ZOLPIDEM TARTRATE - Bryant Ranch PrepackBryant Ranch Prepack2026-07-07HUMAN PRESCRIPTION DRUG LABEL
ZOLPIDEM TARTRATE - Lupin Pharmaceuticals, Inc. | LUPIN LIMITEDLupin Pharmaceuticals, Inc. | LUPIN LIMITED2025-12-26HUMAN PRESCRIPTION DRUG LABEL
ZOLPIDEM TARTRATE - Preferred Pharmaceuticals Inc.Preferred Pharmaceuticals Inc.2025-10-08HUMAN PRESCRIPTION DRUG LABEL
ZOLPIDEM TARTRATE - Bryant Ranch PrepackBryant Ranch Prepack2025-08-08HUMAN PRESCRIPTION DRUG LABEL
ZOLPIDEM TARTRATE - Asclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEMAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2025-04-11HUMAN PRESCRIPTION DRUG LABEL
ZOLPIDEM TARTRATE - Aphena Pharma Solutions - Tennessee, LLCAphena Pharma Solutions - Tennessee, LLC2024-06-10HUMAN PRESCRIPTION DRUG LABEL
ZOLPIDEM TARTRATE - Preferred Pharmaceuticals, Inc.Preferred Pharmaceuticals, Inc.2021-09-30HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68180-779-01ZOLPIDEM TARTRATE100 in 1 BOTTLETABLET, EXTENDED RELEASE10022
68180-779-02ZOLPIDEM TARTRATE500 in 1 BOTTLETABLET, EXTENDED RELEASE50022
68180-779-03ZOLPIDEM TARTRATE1000 in 1 BOTTLETABLET, EXTENDED RELEASE100022
68180-779-04ZOLPIDEM TARTRATE100 in 1 BOTTLETABLET, EXTENDED RELEASE10022
68180-779-06ZOLPIDEM TARTRATE30 in 1 BOTTLETABLET, EXTENDED RELEASE3022
68180-779-11ZOLPIDEM TARTRATE10 in 1 BLISTER PACKTABLET, EXTENDED RELEASE1022

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68180-779ZOLPIDEM TARTRATE TABLET, EXTENDED RELEASE [LUPIN PHARMACEUTICALS, INC.]21Current NDC, Legacy NDC, 6 package rows20250125_ac647afe-2fe5-4056-806f-abdd54789b45.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68180-779-01EA - Each68180-779929cef35-eded-4af3-b405-d118a317baf112014-05-02
68180-779-04EA - Each68180-77903bf9093-0169-4a3f-90f9-8fa51b98151312024-06-10

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ZOLPIDEM TARTRATEACTIVE INGREDIENTWY6W63843KZOLPIDEM TARTRATE TABLET, EXTENDED RELEASE [LUPIN PHARMACEUTICALS, INC.]5
ZOLPIDEMACTIVE MOIETY7K383OQI23ZOLPIDEM TARTRATE TABLET, EXTENDED RELEASE [LUPIN PHARMACEUTICALS, INC.]5

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 2 of 6 · 117 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ZOLPIDEM TARTRATEZOLPIDEM TARTRATECalvin Scott & Co., Inc.7da75d2b-905c-4fdf-bc53-1358c64777552026-01-15Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
ZOLPIDEM TARTRATEZOLPIDEM TARTRATEDirect_Rx907c7b18-2638-512c-e053-2995a90ae6fd2026-01-08Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
Zolpidem TartrateZOLPIDEM TARTRATENorthwind Health Company, LLC47212207-52a1-938b-e063-6294a90abca82025-12-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
ZOLPIDEM TARTRATEZOLPIDEM TARTRATENorthwind Health Company, LLC26e20f53-c042-eac0-e063-6394a90acfca2025-12-26Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
ZOLPIDEM TARTRATEZOLPIDEM TARTRATELupin Pharmaceuticals, Inc.ac647afe-2fe5-4056-806f-abdd54789b452025-12-26Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078970
ndc (package): 68180-780-06
ndc (package): 68180-779-04
ndc (package): 68180-779-02
ndc (package): 68180-779-01
ndc (package): 68180-780-04
ndc (package): 68180-779-03
ndc (package): 68180-779-11
ndc (package): 68180-780-01
ndc (package): 68180-779-06
ndc (package): 68180-780-02
ndc (package): 68180-780-11
ndc (package): 68180-780-03
ndc (product): 68180-780
ndc (product): 68180-779
ndc11 (package): 68180077911
rxcui: 854894
rxcui: 854880
spl id: e56668d7-16c2-4618-ba3b-df3853f307e6
spl set id: ac647afe-2fe5-4056-806f-abdd54789b45
unii: WY6W63843K
Zolpidem TartrateZOLPIDEM TARTRATEA-S Medication Solutions91511d2f-7066-49a0-90ea-2940d955c85e2025-11-26Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
Zolpidem TartrateZOLPIDEM TARTRATEA-S Medication Solutionsef72eb73-d058-4ca3-9013-691aae8426fb2025-11-26Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
zolpidem tartrateZOLPIDEM TARTRATEGolden State Medical Supply, Inc.41124767-8ff7-da5d-e063-6394a90a52032025-11-19Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 854894
rxcui: 854880
unii: WY6W63843K
Zolpidem TartrateZOLPIDEM TARTRATEBryant Ranch Prepack8425be72-2bbe-4090-b00e-610f1a1646b12025-11-19Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 854880
unii: WY6W63843K
ZOLPIDEM TARTRATEZOLPIDEM TARTRATECardinal Health 107, LLC83510333-f07d-4b81-a3ae-2801d114bd312025-10-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
zolpidem tartrateZOLPIDEM TARTRATEAlmatica Pharma LLC2f1a3600-9bd6-3651-3ab5-1e4e0b0a39162025-10-09Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
ZOLPIDEM TARTRATEZOLPIDEM TARTRATEPreferred Pharmaceuticals, Inc.a9ac3d4e-f502-41e3-95c0-0d334584566d2025-10-08Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
ZOLPIDEM TARTRATEZOLPIDEM TARTRATEPreferred Pharmaceuticals Inc.76ff87e4-3aa2-439d-8436-d9e6affb33c82025-10-08Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078970
ndc (package): 68788-8654-3
ndc (package): 68788-8654-6
ndc (package): 68788-8654-9
ndc (product): 68788-8654
rxcui: 854894
spl id: 542b2687-71b1-4b46-bf3c-c3f28bfaa724
spl set id: 76ff87e4-3aa2-439d-8436-d9e6affb33c8
unii: WY6W63843K
ZOLPIDEM TARTRATEZOLPIDEM TARTRATEPreferred Pharmaceuticals, Inc..72e19b8e-d13a-4824-aee4-11778eba552c2025-10-08Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078970
rxcui: 854880
unii: WY6W63843K
Zolpidem TartrateZOLPIDEM TARTRATEPreferred Pharmaceuticals Inc.625fad5b-8817-4773-a2fc-20b662140e6e2025-10-08Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 854880
unii: WY6W63843K
ZOLPIDEM TARTRATEZOLPIDEM TARTRATEBryant Ranch Prepack028bf425-7a72-464d-a242-aa5deee1ac232025-08-08Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA078970
ndc (package): 71335-2764-1
ndc (product): 71335-2764
rxcui: 854894
spl id: 50f6e01a-d753-46ff-9e4c-dd101ebe824e
spl set id: 028bf425-7a72-464d-a242-aa5deee1ac23
unii: WY6W63843K
Zolpidem TartrateZOLPIDEM TARTRATEST. MARY'S MEDICAL PARK PHARMACY3bc8a122-aa21-212c-e063-6394a90a3bda2025-08-07Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
Zolpidem TartrateZOLPIDEM TARTRATEAsclemed USA, Inc.9922ce14-b418-4235-9c59-d674a8e702102025-07-24Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
ZOLPIDEM TARTRATEZOLPIDEM TARTRATEAphena Pharma Solutions - Tennessee, LLC3882d72d-686b-406b-e063-6294a90a0b892025-06-26Boxed warning, Warnings, Adverse reactionsExact identifier
unii: WY6W63843K
Zolpidem TartrateZOLPIDEM TARTRATEAphena Pharma Solutions - Tennessee, LLCa1faca42-6e46-4586-97ac-050b724e7d2a2025-06-09Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 854894
unii: WY6W63843K

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.