meclizine hydrochloride

Generic: meclizine hydrocloride

Labeler: st. mary's medical park pharmacy
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrocloride
Labeler st. mary's medical park pharmacy
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
St. Mary's Medical Park Pharmacy

Identifiers & Regulatory

Product NDC 60760-087
Product ID 60760-087_ef545c37-addf-340f-e053-2995a90aad16
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040659
Listing Expiration 2026-12-31
Marketing Start 2019-04-18

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60760087
Hyphenated Format 60760-087

Supplemental Identifiers

RxCUI
995666
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 hydrocloride (source: ndc)
Application Number ANDA040659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (60760-087-90)
source: ndc

Packages (1)

60760-087-90 90 TABLET in 1 BOTTLE, PLASTIC (60760-087-90)

Ingredients (1)

meclizine hydrochloride (25 mg/1)

Linked Drug Pages (1)

MECLIZINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ef545c37-addf-340f-e053-2995a90aad16", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["87210edf-0bf9-2577-e053-2991aa0aaceb"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-087-90)", "package_ndc": "60760-087-90", "marketing_start_date": "20190418"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "60760-087_ef545c37-addf-340f-e053-2995a90aad16", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "60760-087", "generic_name": "Meclizine Hydrocloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040659", "marketing_category": "ANDA", "marketing_start_date": "20190418", "listing_expiration_date": "20261231"}