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 TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
Medtech Products Inc.

Identifiers & Regulatory

Product NDC 63029-906
Product ID 63029-906_4c3ea8e1-d98a-45c3-9bce-b85dfe8044a4
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009
Listing Expiration 2026-12-31
Marketing Start 2019-02-15

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63029906
Hyphenated Format 63029-906

Supplemental Identifiers

RxCUI
995632 2176732
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
  • 25 mg/1
source: ndc
Packaging
  • 12 TABLET, CHEWABLE in 1 BLISTER PACK (63029-906-12)
source: ndc

Packages (1)

63029-906-12 12 TABLET, CHEWABLE in 1 BLISTER PACK (63029-906-12)

Ingredients (1)

meclizine hydrochloride (25 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": "4c3ea8e1-d98a-45c3-9bce-b85dfe8044a4", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995632", "2176732"], "spl_set_id": ["f8cf751a-9f19-4744-a350-cd22303435ee"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, CHEWABLE in 1 BLISTER PACK (63029-906-12)", "package_ndc": "63029-906-12", "marketing_start_date": "20190215"}], "brand_name": "DRAMAMINE", "product_id": "63029-906_4c3ea8e1-d98a-45c3-9bce-b85dfe8044a4", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "63029-906", "generic_name": "MECLIZINE HYDROCHLORIDE", "labeler_name": "Medtech Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DRAMAMINE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190215", "listing_expiration_date": "20261231"}