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
Label	Manufacturer	Effective date	Type
CARBAMAZEPINE - REMEDYREPACK INC.	REMEDYREPACK INC.	2026-09-28	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Apotex Corp.	Apotex Corp.	2026-08-26	HUMAN PRESCRIPTION DRUG LABEL
Carbamazepine - American Health Packaging	American Health Packaging	2026-08-26	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch Prepack	Bryant Ranch Prepack	2026-03-25	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Preferred Pharmaceuticals Inc.	Preferred Pharmaceuticals Inc.	2026-03-20	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Golden State Medical Supply, Inc.	Golden State Medical Supply, Inc.	2025-11-25	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch Prepack	Bryant Ranch Prepack	2025-07-28	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch Prepack	Bryant Ranch Prepack	2024-04-04	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Bryant Ranch Prepack	Bryant Ranch Prepack	2022-06-06	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE TABLETS, USP 200 mg	NuCare Pharmaceuticals,Inc.	2021-02-16	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE 200mg	RedPharm Drug, Inc.	2021-01-13	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - A-S Medication Solutions	A-S Medication Solutions	2020-01-18	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Proficient Rx LP	Proficient Rx LP	2019-10-01	HUMAN PRESCRIPTION DRUG LABEL
CARBAMAZEPINE - Northwind Pharmaceuticals, LLC	Northwind Pharmaceuticals, LLC	2015-03-23	HUMAN PRESCRIPTION DRUG LABEL
Carbamazepine - State of Florida DOH Central Pharmacy	State of Florida DOH Central Pharmacy	2010-05-20	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
60505-0183-0	CARBAMAZEPINE	100 in 1 BOTTLE	TABLET	100	20
60505-0183-1	CARBAMAZEPINE	1000 in 1 BOTTLE	TABLET	1000	20
60505-0183-5	CARBAMAZEPINE	500 in 1 BOTTLE	TABLET	500	20

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
60505-0183	CARBAMAZEPINE TABLET [APOTEX CORP.]	18	Current NDC, Legacy NDC, 3 package rows	20240206_bf0d012f-da14-8ce3-d74f-56172cddebc5.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
60505-0183-0	EA - Each	60505-0183	22e3a572-b45e-4e44-ba52-b2b381b619ea	1	2012-07-24
60505-0183-1	EA - Each	60505-0183	09301317-1e9a-4408-b724-90fe516c7baa	1	2012-07-24
60505-0183-5	EA - Each	60505-0183	bcc23229-5588-4f23-a06c-02c3a8a72310	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CARBAMAZEPINE	ACTIVE INGREDIENT	33CM23913M	CARBAMAZEPINE TABLET [APOTEX CORP.]	8
CARBAMAZEPINE	ACTIVE MOIETY	33CM23913M	CARBAMAZEPINE TABLET [APOTEX CORP.]	8
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	CARBAMAZEPINE TABLET [APOTEX CORP.]	8
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	CARBAMAZEPINE TABLET [APOTEX CORP.]	8
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CARBAMAZEPINE TABLET [APOTEX CORP.]	8
CARBAMAZEPINE	ACTIVE INGREDIENT	33CM23913M	CARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]	2
CARBAMAZEPINE	ACTIVE MOIETY	33CM23913M	CARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	CARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	CARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CARBAMAZEPINE TABLET [AMERICAN HEALTH PACKAGING]	2
CARBAMAZEPINE	ACTIVE INGREDIENT	33CM23913M	CARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
CARBAMAZEPINE	ACTIVE INGREDIENT	33CM23913M	CARBAMAZEPINE TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1
CARBAMAZEPINE	ACTIVE INGREDIENT	33CM23913M	CARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	1
CARBAMAZEPINE	ACTIVE MOIETY	33CM23913M	CARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
CARBAMAZEPINE	ACTIVE MOIETY	33CM23913M	CARBAMAZEPINE TABLET [NORTHWIND PHARMACEUTICALS, LLC]	1
CARBAMAZEPINE	ACTIVE MOIETY	33CM23913M	CARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	CARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	CARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	CARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	CARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
ETHYLCELLULOSE	INACTIVE INGREDIENT	7Z8S9VYZ4B	CARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
HYPROMELLOSE	INACTIVE INGREDIENT	3NXW29V3WO	CARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	CARBAMAZEPINE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CARBAMAZEPINE TABLET [GOLDEN STATE MEDICAL SUPPLY, INC.]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CARBAMAZEPINE 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 3 of 6 · 117 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Exovisse Preservative-Free Artificial Tears	LUBRICANT EYE GEL DROPS	YD BIO USA, INC.	4f20191a-9124-2525-e063-6294a90a8428	2026-04-10	Warnings	Exact identifier unii: 3NXW29V3WO
LensMate Preservative-Free Artificial Tears	LUBRICANT EYE DROPS	YD BIO USA, INC.	4ebacb2b-9b2d-6bc1-e063-6294a90a3426	2026-04-05	Warnings	Exact identifier unii: 3NXW29V3WO
Exovisse Preservative-Free Artificial Tears	LUBRICANT EYE GEL DROPS	YD BIO USA, INC.	4ebc154b-128b-9dde-e063-6294a90ae00e	2026-04-05	Warnings	Exact identifier unii: 3NXW29V3WO
CARBAMAZEPINE	CARBAMAZEPINE	Bryant Ranch Prepack	c72a0668-7cd7-46a8-86d1-d3c17c4b900f	2026-04-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 33CM23913M
Crocodile Tears Lubricant Eye Drops	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	Crocodile Tears LLC	4df29336-ea0c-0484-e063-6294a90a685a	2026-03-26	Warnings	Exact identifier unii: 3NXW29V3WO
Artificial Tears Lubricant Eye Drops	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	KC Pharmaceuticals, Inc	4de5c844-85ca-ff9f-e063-6394a90ac12c	2026-03-25	Warnings	Exact identifier unii: 3NXW29V3WO
CARBAMAZEPINE	CARBAMAZEPINE	Bryant Ranch Prepack	34f57a68-57ad-57f1-e063-6394a90a3d33	2026-03-25	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA075948 ndc (package): 72162-1708-1 ndc (product): 72162-1708 rxcui: 308979 spl id: e5e7872f-9f37-466f-a6e9-92080cb1c5b7 spl set id: 34f57a68-57ad-57f1-e063-6394a90a3d33 unii: 33CM23913M
Carbamazepine	CARBAMAZEPINE	Preferred Pharmaceuticals Inc.	867a5f4d-8ae6-4339-bbb4-0bf62fb082e5	2026-03-20	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 308979 unii: 33CM23913M
CARBAMAZEPINE	CARBAMAZEPINE	Preferred Pharmaceuticals Inc.	32dc301e-881d-47b0-ad16-f9ff31d19324	2026-03-20	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA075948 ndc (package): 68788-7210-2 ndc (package): 68788-7210-9 ndc (package): 68788-7210-3 ndc (package): 68788-7210-1 ndc (package): 68788-7210-6 ndc (package): 68788-7210-8 ndc (product): 68788-7210 rxcui: 308979 spl id: fc6363d3-830f-49b8-8aea-e34f47ead0d1 spl set id: 32dc301e-881d-47b0-ad16-f9ff31d19324 unii: 33CM23913M
Artificial Tears	GLYCERIN	Preferred Pharmaceuticals Inc.	dd646c72-8f47-43c6-a734-db0dcc8cd4d1	2026-03-06	Warnings	Exact identifier unii: 3NXW29V3WO
Carbamazepine	CARBAMAZEPINE	Northstar Rx LLC	b563e4a1-d7dd-4901-ad45-614f85687589	2026-02-26	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 33CM23913M
Carbamazepine	CARBAMAZEPINE	Golden State Medical Supply, Inc.	536811ab-308b-4866-9185-9e4149483512	2026-02-19	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA075687 unii: 33CM23913M
Carbamazepine	CARBAMAZEPINE	Golden State Medical Supply, Inc.	1922a7cd-6a43-dab5-e063-6294a90a3d8f	2026-02-18	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 33CM23913M
Carbamazepine	CARBAMAZEPINE	Golden State Medical Supply, Inc.	8a1ce79d-18ea-f30b-e053-2995a90ad1fb	2026-02-12	Boxed warning, Warnings, Adverse reactions	Exact identifier application number: ANDA074649 rxcui: 308979 unii: 33CM23913M
Carbamazepine	CARBAMAZEPINE	Bryant Ranch Prepack	47d0ea82-9974-4d41-9ae1-5f1b11419a33	2026-02-12	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 33CM23913M
Carbamazepine	CARBAMAZEPINE	ANI Pharmaceuticals, Inc.	e006049f-1c0c-4544-969e-0344d1b8c5ba	2026-01-26	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 33CM23913M
daa73a0d-9171-4562-8d96-5490c3b94c0e			9f0a6cd8-7274-4983-a4fc-c6617f2b3c8a	2026-01-16	Boxed warning, Warnings, Adverse reactions	Exact identifier spl set id: 9f0a6cd8-7274-4983-a4fc-c6617f2b3c8a
Carbamazepine ER	CARBAMAZEPINE	Epic Pharma, LLC	46a9771e-5830-4905-b5fc-5d1c61fd56a0	2026-01-15	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 33CM23913M
Carbamazepine	CARBAMAZEPINE	AvPAK	ceb84aa4-2041-6e6e-e053-2995a90a0f24	2026-01-08	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 33CM23913M
47e389bd-5a8c-e352-e063-6394a90a80d9			8e5df2e3-92fc-4865-97de-1da0a32c788d	2026-01-08	Boxed warning, Warnings, Adverse reactions	Exact identifier spl set id: 8e5df2e3-92fc-4865-97de-1da0a32c788d

Reported adverse events (FAERS/openFDA)#

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