meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2574
Product ID 68071-2574_49617f72-cc26-7c0d-e063-6294a90ac558
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M009
Listing Expiration 2027-12-31
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 680712574
Hyphenated Format 68071-2574

Supplemental Identifiers

RxCUI
995632
UPC
0368071257427
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
  • 20 TABLET, CHEWABLE in 1 BOTTLE (68071-2574-2)
  • 30 TABLET, CHEWABLE in 1 BOTTLE (68071-2574-3)
  • 60 TABLET, CHEWABLE in 1 BOTTLE (68071-2574-6)
source: ndc

Packages (3)

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": "49617f72-cc26-7c0d-e063-6294a90ac558", "openfda": {"upc": ["0368071257427"], "unii": ["HDP7W44CIO"], "rxcui": ["995632"], "spl_set_id": ["d0d8b376-8fe9-8776-e053-2a95a90ae651"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, CHEWABLE in 1 BOTTLE (68071-2574-2)", "package_ndc": "68071-2574-2", "marketing_start_date": "20211115"}, {"sample": false, "description": "30 TABLET, CHEWABLE in 1 BOTTLE (68071-2574-3)", "package_ndc": "68071-2574-3", "marketing_start_date": "20211115"}, {"sample": false, "description": "60 TABLET, CHEWABLE in 1 BOTTLE (68071-2574-6)", "package_ndc": "68071-2574-6", "marketing_start_date": "20211115"}], "brand_name": "Meclizine Hydrochloride", "product_id": "68071-2574_49617f72-cc26-7c0d-e063-6294a90ac558", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "68071-2574", "generic_name": "Meclizine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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": "20271231"}