meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7873
Product ID 68788-7873_cd73003a-7807-4fe4-9a7c-96534c29ac27
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009
Listing Expiration 2026-12-31
Marketing Start 2021-02-19

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887873
Hyphenated Format 68788-7873

Supplemental Identifiers

RxCUI
995632
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 hydrochloride (source: ndc)
Application Number M009 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET, CHEWABLE in 1 BOTTLE (68788-7873-1)
  • 30 TABLET, CHEWABLE in 1 BOTTLE (68788-7873-2)
source: ndc

Packages (2)

68788-7873-1 100 TABLET, CHEWABLE in 1 BOTTLE (68788-7873-1) 68788-7873-2 30 TABLET, CHEWABLE in 1 BOTTLE (68788-7873-2)

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": "cd73003a-7807-4fe4-9a7c-96534c29ac27", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995632"], "spl_set_id": ["54731aaf-d413-4976-b040-40c8e3e7eafd"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (68788-7873-1)", "package_ndc": "68788-7873-1", "marketing_start_date": "20210219"}, {"sample": false, "description": "30 TABLET, CHEWABLE in 1 BOTTLE (68788-7873-2)", "package_ndc": "68788-7873-2", "marketing_start_date": "20220826"}], "brand_name": "Meclizine Hydrochloride", "product_id": "68788-7873_cd73003a-7807-4fe4-9a7c-96534c29ac27", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "68788-7873", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210219", "listing_expiration_date": "20261231"}