dramamine
Generic: meclizine hydrochloride
Labeler: medtech products inc.Drug Facts
Product Profile
Brand Name
dramamine
Generic Name
meclizine hydrochloride
Labeler
medtech products inc.
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
meclizine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63029-914
Product ID
63029-914_46c83b4e-9f3a-4c67-a759-864e16c5506a
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63029914
Hyphenated Format
63029-914
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 (source: ndc)
Generic Name
meclizine hydrochloride (source: ndc)
Application Number
M009 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 1 BLISTER PACK in 1 BOX (63029-914-12) / 12 TABLET, CHEWABLE 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": "46c83b4e-9f3a-4c67-a759-864e16c5506a", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995632", "2176732"], "spl_set_id": ["fdcbcc4e-9370-4975-8905-1f12c73fdc8c"], "manufacturer_name": ["Medtech Products Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 BOX (63029-914-12) / 12 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "63029-914-12", "marketing_start_date": "20260202"}], "brand_name": "DRAMAMINE", "product_id": "63029-914_46c83b4e-9f3a-4c67-a759-864e16c5506a", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "63029-914", "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": "20260202", "listing_expiration_date": "20261231"}