dramamine

Generic: meclizine hydrochloride

Labeler: medtech products inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name dramamine
Generic Name meclizine hydrochloride
Labeler medtech products inc.
Dosage Form POWDER
Routes
ORAL
Active Ingredients

meclizine dihydrochloride 50 mg/1

Manufacturer
Medtech Products Inc.

Identifiers & Regulatory

Product NDC 63029-912
Product ID 63029-912_871f81c0-8d71-4ff5-8317-9a1f74ba7b83
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009
Listing Expiration 2026-12-31
Marketing Start 2026-02-02

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63029912
Hyphenated Format 63029-912

Supplemental Identifiers

RxCUI
2734132 2734137
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 dramamine (source: ndc)
Generic Name meclizine hydrochloride (source: ndc)
Application Number M009 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 4 POWDER in 1 BOX (63029-912-04)
source: ndc

Packages (1)

63029-912-04 4 POWDER in 1 BOX (63029-912-04)

Ingredients (1)

meclizine dihydrochloride (50 mg/1)

Linked Drug Pages (1)

DRAMAMINE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "871f81c0-8d71-4ff5-8317-9a1f74ba7b83", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["2734132", "2734137"], "spl_set_id": ["6efd3473-ee14-4ee0-8a58-d15a64a9224a"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 POWDER in 1 BOX (63029-912-04)", "package_ndc": "63029-912-04", "marketing_start_date": "20260202"}], "brand_name": "DRAMAMINE", "product_id": "63029-912_871f81c0-8d71-4ff5-8317-9a1f74ba7b83", "dosage_form": "POWDER", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "63029-912", "generic_name": "MECLIZINE HYDROCHLORIDE", "labeler_name": "Medtech Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DRAMAMINE", "active_ingredients": [{"name": "MECLIZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260202", "listing_expiration_date": "20261231"}