Meclizine Hydrochloride

Product NDC: 67296-1432
11-digit product format: 672961432
Labeler code: 67296
Product ID: 67296-1432_be621dfb-bc78-4b5b-e053-2a95a90ae957
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Meclizine Hydrochloride
Dosage form: TABLET
Route: ORAL
Labeler: RedPharm Drug, Inc.
Application: NDA010721
Marketing category: NDA AUTHORIZED GENERIC
Marketing start: 2020-01-15
Marketing end: 0000-00-00
Substance: MECLIZINE HYDROCHLORIDE
Active strength: 25 mg/1
Pharmacologic classes: Antiemetic [EPC],Emesis Suppression [PE]
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Source date
excluded product	product	67296-1432		I	Inactivated by FDA	2026-07-31
excluded package	package	67296-1432	67296-1432-3	I	Inactivated by FDA	2026-07-31
excluded package	package	67296-1432	67296-1432-7	I	Inactivated by FDA	2026-07-31

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 4 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
N010721-001	ANTIVERT	MECLIZINE HYDROCHLORIDE	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	AA	RLD, RS	1982-01-20
N010721-004	ANTIVERT	MECLIZINE HYDROCHLORIDE	25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	AA	RLD, Approved before 1982
N010721-005	ANTIVERT	MECLIZINE HYDROCHLORIDE	25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, CHEWABLE / ORAL		RLD, RS, Approved before 1982
N010721-006	ANTIVERT	MECLIZINE HYDROCHLORIDE	12.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	AA	RLD, Approved before 1982

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 3 matching rows.

Application-product, TE code table
Application-product	TE code
N010721-001	AA
N010721-004	AA
N010721-006	AA

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Product TE source text	RLD / RS	Approval date	Source SHA-256
2026-08-01 22:54:32	2026-06	N010721-001	ANTIVERT	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	AA	RLD, RS	1982-01-20	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	N010721-004	ANTIVERT	25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	AA	RLD, Approved before 1982		`a50c72e98297…`
2026-08-01 22:54:32	2026-06	N010721-005	ANTIVERT	25MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, CHEWABLE / ORAL		RLD, RS, Approved before 1982		`a50c72e98297…`
2026-08-01 22:54:32	2026-06	N010721-006	ANTIVERT	12.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	AA	RLD, Approved before 1982		`a50c72e98297…`

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2026-08-01 22:54:32	2026-06	N010721-001	AA	1	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	N010721-004	AA	1	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	N010721-006	AA	1	`a50c72e98297…`

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 16 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	St. Mary's Medical Park Pharmacy	c6b3f4d8-5fcf-2278-e053-2a95a90ab139	2026-06-21	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Preferred Pharmaceuticals Inc.	d7d31433-8f39-4fe6-b542-1b4410122db7	2026-06-12	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Bryant Ranch Prepack	81e1762b-e012-4c6d-96e6-9a9f27a1880a	2026-05-27	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	REMEDYREPACK INC.	21d4a6ee-0a66-45d7-bab9-c5eef399713d	2026-05-13	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	REMEDYREPACK INC.	d53bf04e-5cfc-4974-9b24-2cce545d1bd0	2026-04-15	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	NuCare Pharmaceuticals,Inc.	c31846b2-d47d-a97b-e053-2a95a90a9bec	2026-03-27	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	NuCare Pharmaceuticals,Inc.	beb36d86-9fb7-1f60-e053-2995a90aac13	2026-03-02	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Bryant Ranch Prepack	112103bc-25e2-42cf-8542-ba1d3392a2c3	2025-08-20	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Bryant Ranch Prepack	27b6a7e0-a361-4705-9f31-719063a65f22	2025-08-20	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Rising Pharma Holdings, Inc.	c9ddc39c-bc6b-42f1-8c5f-5aff2d79c4bd	2025-06-02	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Advanced Rx of Tennessee, LLC	2d31ae73-3f09-a77c-e063-6294a90ade9a	2025-02-02	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
MECLIZINE HYDROCHLORIDE	MECLIZINE HYDROCHLORIDE	DirectRx	d27fe828-4fee-3ba9-e053-2995a90ae7b6	2025-01-20	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Proficient Rx LP	92e8390b-5173-4aa1-906d-35d2c0eaaaf6	2024-08-01	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Direct_Rx	e79ecf77-0e0a-d7ef-e053-2a95a90a5adf	2024-04-09	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Asclemed USA, Inc.	e6a5df4b-5cbf-4a0c-b38a-f4509c9c17db	2024-04-08	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721
Meclizine Hydrochloride	MECLIZINE HYDROCHLORIDE	Proficient Rx LP	b91435d1-fb95-4939-8478-84e41f44f732	2023-04-01	Warnings, Adverse reactions	Exact identifier application applno (NDA): 010721 application number: NDA010721

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ac6963c4-31c6-325f-ee58-83a0a06597ad	Product name	5	20221206

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
67296-1432-3	2026-01-29	C162847	48780-1	f386c64a-0bbc-0266-e053-dadaa90a7c1a	Meclizine 25mg tabs
67296-1432-7	2026-01-29	C162847	48780-1	f386c64a-0bbc-0266-e053-dadaa90a7c1a	Meclizine 25mg tabs
67296-1432-3	2023-02-15	C162847	48780-1	f386c64a-0bbc-0266-e053-dadaa90a7c1a	Meclizine 25mg tabs
67296-1432-3	2023-01-30	C162847	48780-1	f386c64a-0bbc-0266-e053-dadaa90a7c1a	Meclizine 25mg tabs

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
67296-1432-3	Meclizine Hydrochloride	30 in 1 BOTTLE	TABLET	30		5
67296-1432-7	Meclizine Hydrochloride	21 in 1 BOTTLE	TABLET	21		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67296-1432	MECLIZINE HYDROCHLORIDE TABLET [REDPHARM DRUG, INC.]	5	Legacy NDC, 2 package rows	20240808_be620ef8-5391-5b60-e053-2a95a90a0aa4.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
HDP7W44CIO	MECLIZINE HYDROCHLORIDE	31884-77-2	MECLIZINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
995666	meclizine HCl 25 MG Oral Tablet	PSN	be620ef8-5391-5b60-e053-2a95a90a0aa4	5
995666	meclizine hydrochloride 25 MG Oral Tablet	SCD	be620ef8-5391-5b60-e053-2a95a90a0aa4	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
67296-1432-3	67296143203	30 TABLET in 1 BOTTLE (67296-1432-3)	30 tablet	2021-03-01	0000-00-00	No	No	Current
67296-1432-7	67296143207	21 in 1 BOTTLE						Historical

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Meclizine 25mg tabs	RedPharm Drug, Inc. \| RedPharm Drug	2024-08-07	HUMAN PRESCRIPTION DRUG LABEL	5