NDC 68071-3632-01 - acetaZOLAMIDE

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: 68071-3632
Requested NDC: 68071-3632-01
Package NDCs from labels: 68071-3632-1, 68071-3632-01
Manufacturer: NuCare Pharmaceuticals,Inc.
Effective date: 2024-08-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
acetaZOLAMIDE Tablets, USP RX Only	NuCare Pharmaceuticals,Inc.	2024-08-09	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68071-3632-1	acetaZOLAMIDE	100 in 1 BOTTLE	TABLET	100		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68071-3632	ACETAZOLAMIDE TABLET [NUCARE PHARMACEUTICALS,INC.]	2	Current NDC, 1 package rows	20240810_1b2c973f-82ef-a4f3-e063-6394a90aaae0.zip

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 3 · 51 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Acetazolamide	ACETAZOLAMIDE	Chartwell RX, LLC	f75bbf55-98ac-4f91-b6fd-17b5ac860e55	2024-10-10	Warnings, Adverse reactions	Exact identifier rxcui: 197303 rxcui: 197304 unii: O3FX965V0I
acetazolamide	ACETAZOLAMIDE	Zydus Pharmaceuticals (USA) Inc.	bf514e99-4958-44a0-a87a-02a950f87e60	2024-10-08	Warnings, Adverse reactions	Exact identifier unii: O3FX965V0I
acetazolamide	ACETAZOLAMIDE	Zydus Lifesciences Limited	2c1d9078-c15f-4dce-bc26-edfa5400fa9b	2024-10-08	Warnings, Adverse reactions	Exact identifier unii: O3FX965V0I
Acetazolamide	ACETAZOLAMIDE	Alembic Pharmaceuticals Inc.	43231abb-2a5d-44ab-b3e6-7564a1131ac5	2024-09-30	Warnings, Adverse reactions	Exact identifier unii: O3FX965V0I
acetaZOLAMIDE	ACETAZOLAMIDE	NuCare Pharmaceuticals,Inc.	1b2c973f-82ef-a4f3-e063-6394a90aaae0	2024-08-09	Warnings, Adverse reactions	Exact identifier application number: ANDA211069 ndc (package): 68071-3632-1 ndc (product): 68071-3632 ndc11 (package): 68071363201 rxcui: 197303 spl id: 1f42392a-ef99-86c1-e063-6294a90ae0af spl set id: 1b2c973f-82ef-a4f3-e063-6394a90aaae0 unii: O3FX965V0I
acetaZOLAMIDE	ACETAZOLAMIDE	Zydus Pharmaceuticals (USA) Inc.	85e4d8f6-1e82-4068-a768-752287d4ccf2	2024-03-26	Warnings, Adverse reactions	Exact identifier application number: ANDA211069 rxcui: 197303 rxcui: 197304 unii: O3FX965V0I
Pure Cornstarch Baby	CORN STARCH	Walgreen Company	d0e9bd13-b568-4f7e-b036-8d23e71ad8bf	2024-03-25	Warnings	Exact identifier unii: O8232NY3SJ
ACETAZOLAMIDE EXTENDED-RELEASE	ACETAZOLAMIDE EXTENDED-RELEASE	AvPAK	e43f991d-15b9-1e66-e053-2a95a90a9449	2024-01-09	Warnings, Adverse reactions	Exact identifier unii: O3FX965V0I
ACETAZOLAMIDE	ACETAZOLAMIDE	TRUPHARMA, LLC	4fcd428a-7bf3-4e75-a834-1bdf1078107f	2022-06-13	Warnings, Adverse reactions	Exact identifier rxcui: 197303 rxcui: 197304 unii: O3FX965V0I
Acetazolamide	ACETAZOLAMIDE	Proficient Rx LP	3cdde6aa-c89d-4ea4-aade-6c8b5c3ffdcc	2019-10-01	Warnings, Adverse reactions	Exact identifier rxcui: 197303 unii: O3FX965V0I
Acetazolamide	ACETAZOLAMIDE	Alembic Pharmaceuticals Limited	d9c1cc75-4e3d-4eaf-87c5-d5942a843818	2019-02-20	Warnings, Adverse reactions	Exact identifier unii: O3FX965V0I

Reported adverse events (FAERS/openFDA)#

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