FDA.reportPublic FDA data

NDC 60505-0183-01 - CARBAMAZEPINE

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
60505-0183
Requested NDC
60505-0183-01
Package NDCs from labels
60505-0183-0, 60505-0183-5, 60505-0183-1, 60505-0183-01
Manufacturer
REMEDYREPACK INC.
Effective date
2026-09-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
CARBAMAZEPINE - REMEDYREPACK INC.REMEDYREPACK INC.2026-09-28HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Golden State Medical Supply, Inc.Golden State Medical Supply, Inc.2026-09-24HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Apotex Corp.Apotex Corp.2026-08-26HUMAN PRESCRIPTION DRUG LABEL
Carbamazepine - American Health PackagingAmerican Health Packaging2026-08-26HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch PrepackBryant Ranch Prepack2026-03-25HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Preferred Pharmaceuticals Inc.Preferred Pharmaceuticals Inc.2026-03-20HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch PrepackBryant Ranch Prepack2025-07-28HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch PrepackBryant Ranch Prepack2024-04-04HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch PrepackBryant Ranch Prepack2022-06-06HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE TABLETS, USP 200 mgNuCare Pharmaceuticals,Inc.2021-02-16HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE 200mgRedPharm Drug, Inc.2021-01-13HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - A-S Medication SolutionsA-S Medication Solutions2020-01-18HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Proficient Rx LPProficient Rx LP2019-10-01HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Northwind Pharmaceuticals, LLCNorthwind Pharmaceuticals, LLC2015-03-23HUMAN PRESCRIPTION DRUG LABEL
Carbamazepine - State of Florida DOH Central PharmacyState of Florida DOH Central Pharmacy2010-05-20HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60505-0183-0CARBAMAZEPINE100 in 1 BOTTLETABLET10020
60505-0183-1CARBAMAZEPINE1000 in 1 BOTTLETABLET100020
60505-0183-5CARBAMAZEPINE500 in 1 BOTTLETABLET50020

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60505-0183CARBAMAZEPINE TABLET [APOTEX CORP.]18Current NDC, Legacy NDC, 3 package rows20240206_bf0d012f-da14-8ce3-d74f-56172cddebc5.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60505-0183-0EA - Each60505-018322e3a572-b45e-4e44-ba52-b2b381b619ea12012-07-24
60505-0183-1EA - Each60505-018309301317-1e9a-4408-b724-90fe516c7baa12012-07-24
60505-0183-5EA - Each60505-0183bcc23229-5588-4f23-a06c-02c3a8a7231012012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CARBAMAZEPINEACTIVE INGREDIENT33CM23913MCARBAMAZEPINE TABLET [APOTEX CORP.]8
CARBAMAZEPINEACTIVE MOIETY33CM23913MCARBAMAZEPINE TABLET [APOTEX CORP.]8
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCARBAMAZEPINE TABLET [APOTEX CORP.]8
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48CARBAMAZEPINE TABLET [APOTEX CORP.]8
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CARBAMAZEPINE TABLET [APOTEX CORP.]8
CARBAMAZEPINEACTIVE INGREDIENT33CM23913MCARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]2
CARBAMAZEPINEACTIVE MOIETY33CM23913MCARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]2
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48CARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]2
CARBAMAZEPINEACTIVE INGREDIENT33CM23913MCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
CARBAMAZEPINEACTIVE INGREDIENT33CM23913MCARBAMAZEPINE TABLET [NORTHWIND PHARMACEUTICALS, LLC]1
CARBAMAZEPINEACTIVE INGREDIENT33CM23913MCARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]1
CARBAMAZEPINEACTIVE MOIETY33CM23913MCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
CARBAMAZEPINEACTIVE MOIETY33CM23913MCARBAMAZEPINE TABLET [NORTHWIND PHARMACEUTICALS, LLC]1
CARBAMAZEPINEACTIVE MOIETY33CM23913MCARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48CARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48CARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
ETHYLCELLULOSEINACTIVE INGREDIENT7Z8S9VYZ4BCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
HYPROMELLOSEINACTIVE INGREDIENT3NXW29V3WOCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XCARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1

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 6 of 6 · 117 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GENTEAL TEARSDEXTRAN 70, GLYCERIN, HYPROMELLOSEA-S Medication Solutionsa2b715e9-332d-4f0b-b8e5-ebc0006815862024-01-21WarningsExact identifier
unii: 3NXW29V3WO
Equate Eye Drops Dry Eye ReliefGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400Wal-Mart Stores, Inc.91fb8fb5-b871-4535-e053-2995a90a9b162023-12-23WarningsExact identifier
unii: 3NXW29V3WO
Sunmark Dry Eye ReliefGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400Strategic Sourcing Services LLC043ccc34-44ee-416a-88bc-f247774e90752023-12-23WarningsExact identifier
unii: 3NXW29V3WO
Rite Aid Eye Drops Dry Eye ReliefGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400Rite Aid Corporationfa1b5b66-9643-e9a7-e053-6394a90ae3cf2023-12-23WarningsExact identifier
unii: 3NXW29V3WO
Meijer Dry Eye ReliefGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400Meijer Distribution, Inc.9feaa5e2-6aca-96e8-e053-2a95a90a54bd2023-12-22WarningsExact identifier
unii: 3NXW29V3WO
Walgreens Multi-Symptom Relief Eye DropsGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATEWalgreen Co.a03789ce-66bd-7b12-e053-2995a90af85a2023-12-20WarningsExact identifier
unii: 3NXW29V3WO
Walgreens Lubricant Eye Drops Preservative FreeDEXTRAN 70, HYPROMELLOSEWalgreen Company9b383e41-e116-1c12-e053-2a95a90ab25f2023-12-20WarningsExact identifier
unii: 3NXW29V3WO
TopCare Health Dry Eye Relief Eye DropsGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400Topco Associates LLC9c617e34-fc66-1a5b-e053-2995a90ace2c2023-12-20WarningsExact identifier
unii: 3NXW29V3WO
HEB Dry Eye Eye DropsGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400HEBf80023cf-8e42-780a-e053-6294a90a66cd2023-12-20WarningsExact identifier
unii: 3NXW29V3WO
GenTeal Tears (Moderate)DEXTRAN 70, GLYCERIN, HYPROMELLOSEAlcon Laboratories, Inc.a2992597-3490-6a5c-be45-2b6fa15e15472023-12-15WarningsExact identifier
unii: 3NXW29V3WO
CarbamazepineCARBAMAZEPINEUpsher-Smith Laboratories, LLC282c954f-e34a-4bd5-b5eb-771e3c56936f2023-10-19Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 33CM23913M
f70b90cb-7b20-c38e-e053-6294a90aaf097eed4244-61d8-4dbc-b111-10e9997ea4a92023-03-16Boxed warning, Warnings, Adverse reactionsExact identifier
spl set id: 7eed4244-61d8-4dbc-b111-10e9997ea4a9
b8d08b7b-cbff-9efd-e053-2995a90a89e788dd818c-80b5-a85c-e053-2a95a90aa84d2021-01-13Boxed warning, Warnings, Adverse reactionsExact identifier
spl id: b8d08b7b-cbff-9efd-e053-2995a90a89e7
spl set id: 88dd818c-80b5-a85c-e053-2a95a90aa84d
5c28bb65-9313-40e2-9630-cd3302dd3f943554a0b6-ea96-4516-81d7-cc2d27b4fc332020-01-18Boxed warning, Warnings, Adverse reactionsExact identifier
spl id: 5c28bb65-9313-40e2-9630-cd3302dd3f94
spl set id: 3554a0b6-ea96-4516-81d7-cc2d27b4fc33
CARBAMAZEPINECARBAMAZEPINEProficient Rx LPbf61798e-c07e-4959-909a-2b4c2c83b5322019-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA075948
ndc (package): 71205-025-30
ndc (package): 71205-025-60
ndc (package): 71205-025-90
ndc (product): 71205-025
rxcui: 308979
spl id: 9a099066-50bb-4651-bce7-5e1dc8e2e5b1
spl set id: bf61798e-c07e-4959-909a-2b4c2c83b532
unii: 33CM23913M
CARBAMAZEPINECARBAMAZEPINEAphena Pharma Solutions - Tennessee, LLCc1fc31ef-6b2e-4de4-a185-ec44e94e7b402016-06-02Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA075948
rxcui: 308979
unii: 33CM23913M
18def499-cbff-49a0-bdf7-dd5d38fc6f016903e7ef-8b5c-4b64-a87d-62f1f102bc752010-05-20Boxed warning, Warnings, Adverse reactionsExact identifier
spl id: 18def499-cbff-49a0-bdf7-dd5d38fc6f01
spl set id: 6903e7ef-8b5c-4b64-a87d-62f1f102bc75

Reported adverse events (FAERS/openFDA)#

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