NDC 61919-266-30 - 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: 61919-266
Requested NDC: 61919-266-30
Package NDCs from labels: 61919-266-90, 61919-266-30, 61919-266-60
Manufacturer: DIRECT RX
Effective date: 2020-01-20
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
CLONIDINE HYDROCHLORIDE - DIRECT RX	DIRECT RX	2020-01-20	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
61919-266-60	2023-01-30	C162847	48780-1	f386c64a-3b61-0266-e053-dadaa90a7c1a	CLONIDINE HYDROCHLORIDE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
61919-266-30	CLONIDINE HYDROCHLORIDE	30 in 1 BOTTLE	TABLET	30	3
61919-266-60	CLONIDINE HYDROCHLORIDE	60 in 1 BOTTLE	TABLET	60	3
61919-266-90	CLONIDINE HYDROCHLORIDE	90 in 1 BOTTLE	TABLET	90	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61919-266	CLONIDINE HYDROCHLORIDE TABLET [DIRECT RX]	3	Legacy NDC, 3 package rows	20200121_e6583ff5-0e03-470b-a986-35770aa0e80b.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
61919-266-30	EA - Each	61919-266	4f1eb55e-fd95-4679-9e68-1956b75c16f0	1	2014-12-01
61919-266-60	EA - Each	61919-266	fb5612ce-dd07-40c4-8ca1-7de2aa29cba5	1	2015-02-02
61919-266-90	EA - Each	61919-266	96142d10-545a-46a2-b8ba-ffdffa1d5763	1	2015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CLONIDINE HYDROCHLORIDE	ACTIVE INGREDIENT	W76I6XXF06	CLONIDINE HYDROCHLORIDE TABLET [DIRECT RX]	1
CLONIDINE	ACTIVE MOIETY	MN3L5RMN02	CLONIDINE HYDROCHLORIDE TABLET [DIRECT RX]	1
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	CLONIDINE HYDROCHLORIDE TABLET [DIRECT RX]	1
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	CLONIDINE HYDROCHLORIDE TABLET [DIRECT RX]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	CLONIDINE HYDROCHLORIDE TABLET [DIRECT RX]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CLONIDINE HYDROCHLORIDE TABLET [DIRECT RX]	1
SODIUM STARCH GLYCOLATE TYPE A POTATO	INACTIVE INGREDIENT	5856J3G2A2	CLONIDINE HYDROCHLORIDE TABLET [DIRECT RX]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	CLONIDINE HYDROCHLORIDE TABLET [DIRECT RX]	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 1 of 6 · 119 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Clonidine Hydrochloride	CLONIDINE HYDROCHLORIDE	REMEDYREPACK INC.	6d7cfb02-e580-4658-a2fe-2149b515d434	2026-09-09	Warnings, Adverse reactions	Exact identifier rxcui: 884189 unii: W76I6XXF06
Clonidine Hydrochloride	CLONIDINE HYDROCHLORIDE	REMEDYREPACK INC.	00c6d67a-bb11-4884-9eeb-4e1b8701a08b	2026-09-08	Warnings, Adverse reactions	Exact identifier application number: ANDA070974 rxcui: 884173 unii: W76I6XXF06
Clonidine Hydrochloride	CLONIDINE HYDROCHLORIDE	REMEDYREPACK INC.	4b889e12-0382-4679-9cec-d6829c59e853	2026-09-08	Warnings, Adverse reactions	Exact identifier rxcui: 884185 unii: W76I6XXF06
QLONILIK	CLONIDINE HYDROCHLORIDE	CMP Pharma, Inc.	826de1dc-378e-4c90-86d1-e33f7a4248cd	2026-08-12	Warnings, Adverse reactions	Exact identifier unii: W76I6XXF06
clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	Coupler LLC	58772b44-dec0-7001-e063-6394a90ac40e	2026-08-07	Warnings, Adverse reactions	Exact identifier rxcui: 884189 unii: W76I6XXF06
clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	REMEDYREPACK INC.	e5d24f52-e0c2-428d-b647-481d63ffd95f	2026-08-04	Warnings, Adverse reactions	Exact identifier rxcui: 884173 unii: W76I6XXF06
clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	Redpharm Drug	53df40e7-dd2b-d40e-e063-6394a90a21c4	2026-07-31	Warnings, Adverse reactions	Exact identifier rxcui: 884173 unii: W76I6XXF06
Clonidine Hydrochloride	CLONIDINE HYDROCHLORIDE	Major Pharmaceuticals	8171776a-dd14-4dcc-8860-3c27d8ea9504	2026-07-27	Warnings, Adverse reactions	Exact identifier rxcui: 884185 rxcui: 884173 unii: W76I6XXF06
clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	REMEDYREPACK INC.	574640a5-829d-4e9d-be32-832a48cbd8dd	2026-07-02	Warnings, Adverse reactions	Exact identifier rxcui: 884173 unii: W76I6XXF06
clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	REMEDYREPACK INC.	2a183d05-5be7-43e9-a084-700ec05d01e9	2026-07-02	Warnings, Adverse reactions	Exact identifier rxcui: 884185 unii: W76I6XXF06
clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	St. Mary's Medical Park Pharmacy	32d72d7b-5881-f431-e063-6394a90a3547	2026-06-26	Warnings, Adverse reactions	Exact identifier rxcui: 884173 unii: W76I6XXF06
Clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	Bryant Ranch Prepack	cee049ea-a476-433c-971f-2466a6a3263b	2026-06-24	Warnings, Adverse reactions	Exact identifier rxcui: 884173 unii: W76I6XXF06
Clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	Bryant Ranch Prepack	f65d90dc-11b4-4d63-b4a9-30603bc332ea	2026-06-24	Warnings, Adverse reactions	Exact identifier rxcui: 884189 unii: W76I6XXF06
Clonidine Hydrochloride	CLONIDINE HYDROCHLORIDE	Unit Dose Solutions, Inc.	547beb0f-0c12-2ef4-e063-6394a90a6a73	2026-06-17	Warnings, Adverse reactions	Exact identifier rxcui: 884185 unii: W76I6XXF06
Clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	Unit Dose Solutions, Inc.	544ea5bf-6713-f034-e063-6394a90a781b	2026-06-15	Warnings, Adverse reactions	Exact identifier rxcui: 884173 unii: W76I6XXF06
Clonidine Hydrochloride	CLONIDINE HYDROCHLORIDE	REMEDYREPACK INC.	7ec53e25-c50a-48b4-82b0-c0b3626f31dc	2026-06-01	Warnings, Adverse reactions	Exact identifier application number: ANDA070974 rxcui: 884173 unii: W76I6XXF06
clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	PD-Rx Pharmaceuticals, Inc.	ea1527a5-4939-4ff7-a827-f88a9113a07d	2026-05-26	Warnings, Adverse reactions	Exact identifier rxcui: 884185 unii: W76I6XXF06
clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	PD-Rx Pharmaceuticals, Inc.	be1b921d-152e-4bd5-82bd-56e2f8beef3e	2026-05-26	Warnings, Adverse reactions	Exact identifier rxcui: 884189 unii: W76I6XXF06
clonidine hydrochloride	CLONIDINE HYDROCHLORIDE	ASCLEMED USA INC.	200afa03-adf3-4dca-8de8-1569701bd029	2026-05-20	Warnings, Adverse reactions	Exact identifier rxcui: 884185 rxcui: 884173 rxcui: 884189 unii: W76I6XXF06
Clonidine Hydrochloride	CLONIDINE HYDROCHLORIDE	Coupler LLC	266af0b1-ce85-6699-e063-6394a90acb4d	2026-05-07	Warnings, Adverse reactions	Exact identifier rxcui: 884185 unii: W76I6XXF06

Reported adverse events (FAERS/openFDA)#

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