meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: aphena pharma solutions - tennessee, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler aphena pharma solutions - tennessee, llc
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
Aphena Pharma Solutions - Tennessee, LLC

Identifiers & Regulatory

Product NDC 71610-836
Product ID 71610-836_1a8bdae4-1b42-0a1c-e063-6294a90a49aa
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009
Listing Expiration 2026-12-31
Marketing Start 2020-10-30

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71610836
Hyphenated Format 71610-836

Supplemental Identifiers

RxCUI
995632
UNII
HDP7W44CIO

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 meclizine hydrochloride (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
  • 30 TABLET, CHEWABLE in 1 BOTTLE (71610-836-30)
  • 60 TABLET, CHEWABLE in 1 BOTTLE (71610-836-53)
  • 90 TABLET, CHEWABLE in 1 BOTTLE (71610-836-60)
  • 180 TABLET, CHEWABLE in 1 BOTTLE (71610-836-80)
source: ndc

Packages (4)

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": "1a8bdae4-1b42-0a1c-e063-6294a90a49aa", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995632"], "spl_set_id": ["199ae195-4556-ee88-e063-6394a90a40d4"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, CHEWABLE in 1 BOTTLE (71610-836-30)", "package_ndc": "71610-836-30", "marketing_start_date": "20240524"}, {"sample": false, "description": "60 TABLET, CHEWABLE in 1 BOTTLE (71610-836-53)", "package_ndc": "71610-836-53", "marketing_start_date": "20240524"}, {"sample": false, "description": "90 TABLET, CHEWABLE in 1 BOTTLE (71610-836-60)", "package_ndc": "71610-836-60", "marketing_start_date": "20240524"}, {"sample": false, "description": "180 TABLET, CHEWABLE in 1 BOTTLE (71610-836-80)", "package_ndc": "71610-836-80", "marketing_start_date": "20240524"}], "brand_name": "Meclizine Hydrochloride", "product_id": "71610-836_1a8bdae4-1b42-0a1c-e063-6294a90a49aa", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "71610-836", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M009", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201030", "listing_expiration_date": "20261231"}