meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler walgreen company
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-5172
Product ID 0363-5172_30139dc7-2c78-271f-e063-6294a90aa001
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009
Listing Expiration 2026-12-31
Marketing Start 2023-03-22

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03635172
Hyphenated Format 0363-5172

Supplemental Identifiers

RxCUI
995632
UNII
HDP7W44CIO

Packaging Origin

Original Packager
true

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
  • 1 BLISTER PACK in 1 CARTON (0363-5172-07) / 12 TABLET, CHEWABLE in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

meclizine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30139dc7-2c78-271f-e063-6294a90aa001", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995632"], "spl_set_id": ["ecf8d05e-0e77-f3e8-e053-2a95a90a6604"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0363-5172-07)  / 12 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "0363-5172-07", "marketing_start_date": "20230322"}], "brand_name": "Meclizine Hydrochloride", "product_id": "0363-5172_30139dc7-2c78-271f-e063-6294a90aa001", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "0363-5172", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Walgreen Company", "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": "20230322", "listing_expiration_date": "20261231"}