dramamine - n

Generic: meclizine hydrochloride

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

Drug Facts

Product Profile

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

meclizine hydrochloride 25 mg/1

Manufacturer
Medtech Products Inc.

Identifiers & Regulatory

Product NDC 63029-905
Product ID 63029-905_101152a8-cb8e-4f6f-b52a-6667b6343a24
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009
Listing Expiration 2026-12-31
Marketing Start 2018-01-15

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63029905
Hyphenated Format 63029-905

Supplemental Identifiers

RxCUI
995666 2110527
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 - n (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
  • 2 BLISTER PACK in 1 BOX (63029-905-10) / 5 TABLET 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": "101152a8-cb8e-4f6f-b52a-6667b6343a24", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666", "2110527"], "spl_set_id": ["7fec7791-c242-4e43-8184-32820e657afb"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 BOX (63029-905-10)  / 5 TABLET in 1 BLISTER PACK", "package_ndc": "63029-905-10", "marketing_start_date": "20180115"}], "brand_name": "DRAMAMINE - N", "product_id": "63029-905_101152a8-cb8e-4f6f-b52a-6667b6343a24", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "63029-905", "generic_name": "MECLIZINE HYDROCHLORIDE", "labeler_name": "Medtech Products Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DRAMAMINE - N", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180115", "listing_expiration_date": "20261231"}