meclizine hydrochloride

Generic: meclizine

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine
Labeler redpharm drug
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2205
Product ID 67296-2205_4727eeb1-e0a4-a92c-e063-6394a90af806
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202640
Listing Expiration 2026-12-31
Marketing Start 2023-09-14

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672962205
Hyphenated Format 67296-2205

Supplemental Identifiers

RxCUI
995666
UNII
HDP7W44CIO

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name meclizine hydrochloride (source: ndc)
Generic Name meclizine (source: ndc)
Application Number ANDA202640 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (67296-2205-3)
source: ndc

Packages (1)

67296-2205-3 30 TABLET in 1 BOTTLE (67296-2205-3)

Ingredients (1)

meclizine hydrochloride (25 mg/1)

Linked Drug Pages (1)

MECLIZINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4727eeb1-e0a4-a92c-e063-6394a90af806", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["4727e7a9-eabb-a2a7-e063-6394a90a8754"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-2205-3)", "package_ndc": "67296-2205-3", "marketing_start_date": "20230914"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "67296-2205_4727eeb1-e0a4-a92c-e063-6394a90af806", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "67296-2205", "generic_name": "MECLIZINE", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA202640", "marketing_category": "ANDA", "marketing_start_date": "20230914", "listing_expiration_date": "20261231"}