motion sickness

Generic: meclizine hcl

Labeler: h e b
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name motion sickness
Generic Name meclizine hcl
Labeler h e b
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-903
Product ID 37808-903_3473b0b6-6443-4b2d-b8b1-89350fc754ad
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009
Listing Expiration 2026-12-31
Marketing Start 2019-06-24

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808903
Hyphenated Format 37808-903

Supplemental Identifiers

RxCUI
995666
UPC
0041220834723
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 motion sickness (source: ndc)
Generic Name meclizine hcl (source: ndc)
Application Number M009 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (37808-903-12)
source: ndc

Packages (1)

37808-903-12 100 TABLET in 1 BOTTLE (37808-903-12)

Ingredients (1)

meclizine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Motion Sickness ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3473b0b6-6443-4b2d-b8b1-89350fc754ad", "openfda": {"upc": ["0041220834723"], "unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["9837e9af-c542-4c0f-be33-94927d67c6a7"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (37808-903-12)", "package_ndc": "37808-903-12", "marketing_start_date": "20190624"}], "brand_name": "Motion Sickness", "product_id": "37808-903_3473b0b6-6443-4b2d-b8b1-89350fc754ad", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "37808-903", "generic_name": "Meclizine HCl", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Motion Sickness", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190624", "listing_expiration_date": "20261231"}