meclizine hcl

Generic: meclizine hydrochloride

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hcl
Generic Name meclizine hydrochloride
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 12.5 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 57237-333
Product ID 57237-333_f603203c-84a4-4b41-a244-cff913e5c2e0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009.50
Listing Expiration 2026-12-31
Marketing Start 2024-07-22

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 57237333
Hyphenated Format 57237-333

Supplemental Identifiers

RxCUI
995624
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 hcl (source: ndc)
Generic Name meclizine hydrochloride (source: ndc)
Application Number M009.50 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (57237-333-01)
source: ndc

Packages (1)

Ingredients (1)

meclizine hydrochloride (12.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f603203c-84a4-4b41-a244-cff913e5c2e0", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624"], "spl_set_id": ["acdf636c-66f1-4a1f-87a8-786f51d75708"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (57237-333-01)", "package_ndc": "57237-333-01", "marketing_start_date": "20240722"}], "brand_name": "Meclizine HCl", "product_id": "57237-333_f603203c-84a4-4b41-a244-cff913e5c2e0", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "57237-333", "generic_name": "MECLIZINE HYDROCHLORIDE", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Meclizine HCl", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "M009.50", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240722", "listing_expiration_date": "20261231"}