FDA.reportPublic FDA data

NDC 68071-4545-06 - Clonidine hydrochloride

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
68071-4545
Requested NDC
68071-4545-06
Package NDCs from labels
68071-4545-1, 68071-4545-3, 68071-4545-2, 68071-4545-8, 68071-4545-6, 68071-4545-06
Manufacturer
NuCare Pharmaceuticals,Inc.
Effective date
2026-03-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Clonidine hydrochlorideNuCare Pharmaceuticals,Inc.2026-03-02HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
68071-4545-12024-06-10Clonidine hydrochloride
68071-4545-22024-06-10Clonidine hydrochloride
68071-4545-32024-06-10Clonidine hydrochloride
68071-4545-82024-06-10Clonidine hydrochloride
68071-4545-12023-01-30Clonidine hydrochloride
68071-4545-22023-01-30Clonidine hydrochloride
68071-4545-32023-01-30Clonidine hydrochloride
68071-4545-82023-01-30Clonidine hydrochloride
68071-4545-12021-02-19Clonidine hydrochloride
68071-4545-22021-02-19Clonidine hydrochloride
68071-4545-32021-02-19Clonidine hydrochloride
68071-4545-82021-02-19Clonidine hydrochloride
68071-4545-12021-01-29Clonidine hydrochloride
68071-4545-22021-01-29Clonidine hydrochloride
68071-4545-32021-01-29Clonidine hydrochloride
68071-4545-82021-01-29Clonidine hydrochloride

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68071-4545-1Clonidine hydrochloride12 in 1 BOTTLETABLET125
68071-4545-2Clonidine hydrochloride120 in 1 BOTTLETABLET1205
68071-4545-3Clonidine hydrochloride30 in 1 BOTTLETABLET305
68071-4545-6Clonidine hydrochloride60 in 1 BOTTLETABLET605
68071-4545-8Clonidine hydrochloride180 in 1 BOTTLETABLET1805

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 1 of 7 · 140 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Clonidine HydrochlorideCLONIDINE HYDROCHLORIDEREMEDYREPACK INC.6d7cfb02-e580-4658-a2fe-2149b515d4342026-09-09Warnings, Adverse reactionsExact identifier
rxcui: 884189
unii: W76I6XXF06
Clonidine HydrochlorideCLONIDINE HYDROCHLORIDEREMEDYREPACK INC.00c6d67a-bb11-4884-9eeb-4e1b8701a08b2026-09-08Warnings, Adverse reactionsExact identifier
rxcui: 884173
unii: W76I6XXF06
Clonidine HydrochlorideCLONIDINE HYDROCHLORIDEREMEDYREPACK INC.4b889e12-0382-4679-9cec-d6829c59e8532026-09-08Warnings, Adverse reactionsExact identifier
rxcui: 884185
unii: W76I6XXF06
QLONILIKCLONIDINE HYDROCHLORIDECMP Pharma, Inc.826de1dc-378e-4c90-86d1-e33f7a4248cd2026-08-12Warnings, Adverse reactionsExact identifier
unii: W76I6XXF06
clonidine hydrochlorideCLONIDINE HYDROCHLORIDECoupler LLC58772b44-dec0-7001-e063-6394a90ac40e2026-08-07Warnings, Adverse reactionsExact identifier
rxcui: 884189
unii: W76I6XXF06
clonidine hydrochlorideCLONIDINE HYDROCHLORIDEREMEDYREPACK INC.e5d24f52-e0c2-428d-b647-481d63ffd95f2026-08-04Warnings, Adverse reactionsExact identifier
rxcui: 884173
unii: W76I6XXF06
clonidine hydrochlorideCLONIDINE HYDROCHLORIDERedpharm Drug53df40e7-dd2b-d40e-e063-6394a90a21c42026-07-31Warnings, Adverse reactionsExact identifier
rxcui: 884173
unii: W76I6XXF06
Clonidine HydrochlorideCLONIDINE HYDROCHLORIDEMajor Pharmaceuticals8171776a-dd14-4dcc-8860-3c27d8ea95042026-07-27Warnings, Adverse reactionsExact identifier
rxcui: 884185
rxcui: 884173
unii: W76I6XXF06
clonidine hydrochlorideCLONIDINE HYDROCHLORIDEREMEDYREPACK INC.e96ab74c-eedf-4d71-8a35-d5ec3daa75922026-07-21Warnings, Adverse reactionsExact identifier
rxcui: 884189
unii: W76I6XXF06
clonidine hydrochlorideCLONIDINE HYDROCHLORIDEREMEDYREPACK INC.574640a5-829d-4e9d-be32-832a48cbd8dd2026-07-02Warnings, Adverse reactionsExact identifier
rxcui: 884173
unii: W76I6XXF06
clonidine hydrochlorideCLONIDINE HYDROCHLORIDEREMEDYREPACK INC.2a183d05-5be7-43e9-a084-700ec05d01e92026-07-02Warnings, Adverse reactionsExact identifier
rxcui: 884185
unii: W76I6XXF06
clonidine hydrochlorideCLONIDINE HYDROCHLORIDESt. Mary's Medical Park Pharmacy32d72d7b-5881-f431-e063-6394a90a35472026-06-26Warnings, Adverse reactionsExact identifier
rxcui: 884173
unii: W76I6XXF06
Clonidine hydrochlorideCLONIDINE HYDROCHLORIDEBryant Ranch Prepackcee049ea-a476-433c-971f-2466a6a3263b2026-06-24Warnings, Adverse reactionsExact identifier
application number: ANDA070925
rxcui: 884173
unii: W76I6XXF06
Clonidine hydrochlorideCLONIDINE HYDROCHLORIDEBryant Ranch Prepackf65d90dc-11b4-4d63-b4a9-30603bc332ea2026-06-24Warnings, Adverse reactionsExact identifier
application number: ANDA070923
rxcui: 884189
unii: W76I6XXF06
Clonidine HydrochlorideCLONIDINE HYDROCHLORIDEUnit Dose Solutions, Inc.547beb0f-0c12-2ef4-e063-6394a90a6a732026-06-17Warnings, Adverse reactionsExact identifier
rxcui: 884185
unii: W76I6XXF06
Clonidine hydrochlorideCLONIDINE HYDROCHLORIDEUnit Dose Solutions, Inc.544ea5bf-6713-f034-e063-6394a90a781b2026-06-15Warnings, Adverse reactionsExact identifier
application number: ANDA070923
rxcui: 884173
unii: W76I6XXF06
Clonidine HydrochlorideCLONIDINE HYDROCHLORIDEREMEDYREPACK INC.7ec53e25-c50a-48b4-82b0-c0b3626f31dc2026-06-01Warnings, Adverse reactionsExact identifier
rxcui: 884173
unii: W76I6XXF06
clonidine hydrochlorideCLONIDINE HYDROCHLORIDEPD-Rx Pharmaceuticals, Inc.ea1527a5-4939-4ff7-a827-f88a9113a07d2026-05-26Warnings, Adverse reactionsExact identifier
rxcui: 884185
unii: W76I6XXF06
clonidine hydrochlorideCLONIDINE HYDROCHLORIDEPD-Rx Pharmaceuticals, Inc.be1b921d-152e-4bd5-82bd-56e2f8beef3e2026-05-26Warnings, Adverse reactionsExact identifier
rxcui: 884189
unii: W76I6XXF06
clonidine hydrochlorideCLONIDINE HYDROCHLORIDEASCLEMED USA INC.200afa03-adf3-4dca-8de8-1569701bd0292026-05-20Warnings, Adverse reactionsExact identifier
rxcui: 884185
rxcui: 884173
rxcui: 884189
unii: W76I6XXF06

Reported adverse events (FAERS/openFDA)#

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