meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

meclizine hydrochloride 25 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3791
Product ID 68071-3791_2e0ed208-075d-a301-e063-6294a90a84e2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213957
Listing Expiration 2026-12-31
Marketing Start 2020-10-29

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713791
Hyphenated Format 68071-3791

Supplemental Identifiers

RxCUI
995666
UPC
0368071379129
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 ANDA213957 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (68071-3791-2)
source: ndc

Packages (1)

68071-3791-2 20 TABLET in 1 BOTTLE (68071-3791-2)

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": "2e0ed208-075d-a301-e063-6294a90a84e2", "openfda": {"upc": ["0368071379129"], "unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["2e0ed1fc-53e6-a3b1-e063-6394a90af419"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-3791-2)", "package_ndc": "68071-3791-2", "marketing_start_date": "20250213"}], "brand_name": "Meclizine Hydrochloride", "product_id": "68071-3791_2e0ed208-075d-a301-e063-6294a90a84e2", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "68071-3791", "generic_name": "Meclizine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA213957", "marketing_category": "ANDA", "marketing_start_date": "20201029", "listing_expiration_date": "20261231"}