NDC 68071-3772-06 - Azathioprine

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: 68071-3772
Requested NDC: 68071-3772-06
Package NDCs from labels: 68071-3772-6, 68071-3772-06
Manufacturer: NuCare Pharmaceuticals, Inc.
Effective date: 2025-01-13
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Azathioprine Tablets, USP	NuCare Pharmaceuticals, Inc.	2025-01-13	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68071-3772-6	Azathioprine	60 in 1 BOTTLE	TABLET	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68071-3772	AZATHIOPRINE TABLET [NUCARE PHARMACEUTICALS, INC.]	1	Current NDC, 1 package rows	20250116_2b9f91b9-7959-65e7-e063-6294a90a3680.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 5 of 5 · 83 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Good Neighbor Pharmacy Artifical Tears Lubricant Eye Drops	POLYVINYL ALCOHOL, POVIDONE	Proficient Rx LP	73e12596-6dd5-4cd2-83ed-992e1211b4b8	2023-12-01	Warnings	Exact identifier unii: FZ989GH94E
AZATHIOPRINE	AZATHIOPRINE	Amneal Pharmaceuticals NY LLC	c49b7cc5-0eed-43b7-b7ad-cbb1b6f0cd2c	2021-02-02	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 197388 unii: MRK240IY2L
AZATHIOPRINE	AZATHIOPRINE	Aphena Pharma Solutions - Tennessee, LLC	2f994aed-f8e7-4967-a167-b22b783b4192	2018-09-05	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 197388 unii: MRK240IY2L

Reported adverse events (FAERS/openFDA)#

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