FDA.reportPublic FDA data

Clonidine hydrochloride

Product NDC
68071-4545
Requested package NDC
68071-4545-1
11-digit product format
680714545
Labeler code
68071
Product ID
68071-4545_4c126ce5-07c9-6321-e063-6294a90a5c95
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clonidine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA070925
Marketing category
ANDA
Marketing start
2017-06-01
Substance
CLONIDINE HYDROCHLORIDE
Active strength
.1 mg/1
Pharmacologic classes
Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 15 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source dateCodeStatusSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05DDiscontinued by firmd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26DDiscontinued by firmf5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31DDiscontinued by firm2ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28DDiscontinued by firma1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21DDiscontinued by firmcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10DDiscontinued by firmcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31DDiscontinued by firm302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20DDiscontinued by firmed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10DDiscontinued by firm0efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08DDiscontinued by firmad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03DDiscontinued by firm367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09DDiscontinued by firm557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-28IInactivated by FDA8af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14IInactivated by FDA834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08IInactivated by FDA1332a3947898…d4bfe170f9cd…

Source provenance: Browse the complete Orange Book source catalog.

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Clonidine hydrochloride
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CLONIDINE HYDROCHLORIDE.1 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
W76I6XXF06Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
884173Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
7484e8fa-13a7-70e9-e053-2a91aa0a24b7Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
45c8ba14-e378-46f0-b21f-1aad8e08c613Product name120250221
6920b0ed-30bc-b127-73e1-0713049bd41eProduct name920190618
6920b0ed-30bc-b127-73e1-0713049bd41eProduct name520171212
48f5a4fd-7cdc-dc04-771d-ce7a47326789Product name220150123
624cf764-e200-44b5-83c2-84526255adb5Product name120150107
47972e1b-c905-eeee-5e77-eb4538ad833cProduct name120140508
7667d8e2-e5be-36e1-4de7-231aa7fdaf5cProduct name120140508

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 1 · 7 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Clonidine hydrochlorideCLONIDINE HYDROCHLORIDEBryant Ranch Prepackcee049ea-a476-433c-971f-2466a6a3263b2026-06-24Warnings, Adverse reactionsExact identifier
application applno (ANDA): 070925
application number: ANDA070925
Clonidine hydrochlorideCLONIDINE HYDROCHLORIDENuCare Pharmaceuticals,Inc.50c8a725-a449-256b-e063-6294a90a3e442026-05-01Warnings, Adverse reactionsExact identifier
application applno (ANDA): 070925
application number: ANDA070925
Clonidine hydrochlorideCLONIDINE HYDROCHLORIDENuCare Pharmaceuticals,Inc.7484e8fa-13a7-70e9-e053-2a91aa0a24b72026-03-02Warnings, Adverse reactionsExact identifier
application applno (ANDA): 070925
application number: ANDA070925
ndc (package): 68071-4545-1
ndc (product): 68071-4545
ndc11 (package): 68071454501
Clonidine hydrochlorideCLONIDINE HYDROCHLORIDENorthwind Health Company, LLCdf603f27-d341-3957-e053-2995a90a825f2026-01-01Warnings, Adverse reactionsExact identifier
application applno (ANDA): 070925
application number: ANDA070925
CLONIDINE HYDROCHLORIDECLONIDINE HYDROCHLORIDEProficient Rx LPd072d601-b3d2-46e0-af1f-98adc9572f4a2025-10-01Warnings, Adverse reactionsExact identifier
application applno (ANDA): 070925
application number: ANDA070925
Clonidine hydrochlorideCLONIDINE HYDROCHLORIDEAsclemed USA, Inc.e8c7aa08-1450-de68-e053-2995a90ad0b62022-09-16Warnings, Adverse reactionsExact identifier
application applno (ANDA): 070925
application number: ANDA070925
Clonidine hydrochlorideCLONIDINE HYDROCHLORIDEProficient Rx LP33c68d5e-6a68-40fd-a326-bf36a7e01d5b2022-09-01Warnings, Adverse reactionsExact identifier
application applno (ANDA): 070925
application number: ANDA070925

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
884173cloNIDine HCl 0.1 MG Oral TabletPSN7484e8fa-13a7-70e9-e053-2a91aa0a24b75
884173clonidine hydrochloride 0.1 MG Oral TabletSCD7484e8fa-13a7-70e9-e053-2a91aa0a24b75
884173clonidine HCl 100 MCG Oral TabletSY7484e8fa-13a7-70e9-e053-2a91aa0a24b75

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68071-4545-16807145450112 TABLET in 1 BOTTLE (68071-4545-1) 12 tablet2018-08-280000-00-00NoNoCurrent