dramamine - n
Generic: meclizine hydrochloride
Labeler: medtech products inc.Drug Facts
Product Profile
Brand Name
dramamine - n
Generic Name
meclizine hydrochloride
Labeler
medtech products inc.
Dosage Form
TABLET
Routes
Active Ingredients
meclizine hydrochloride 25 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63029905
Hyphenated Format
63029-905
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 2 BLISTER PACK in 1 BOX (63029-905-10) / 5 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (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"}