meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name meclizine hydrochloride
Generic Name meclizine hydrochloride
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

meclizine hydrochloride 12.5 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 16571-660
Product ID 16571-660_2be27ea6-3d0a-4036-ab42-fea4720daa34
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA010721
Listing Expiration 2026-12-31
Marketing Start 2020-01-15

Pharmacologic Class

Classes
antiemetic [epc] emesis suppression [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16571660
Hyphenated Format 16571-660

Supplemental Identifiers

RxCUI
995624 995632 995666 995686
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 meclizine hydrochloride (source: ndc)
Generic Name meclizine hydrochloride (source: ndc)
Application Number NDA010721 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (16571-660-01)
  • 500 TABLET in 1 BOTTLE (16571-660-50)
source: ndc

Packages (2)

16571-660-01 100 TABLET in 1 BOTTLE (16571-660-01) 16571-660-50 500 TABLET in 1 BOTTLE (16571-660-50)

Ingredients (1)

meclizine hydrochloride (12.5 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": "2be27ea6-3d0a-4036-ab42-fea4720daa34", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995624", "995632", "995666", "995686"], "spl_set_id": ["c9ddc39c-bc6b-42f1-8c5f-5aff2d79c4bd"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-660-01)", "package_ndc": "16571-660-01", "marketing_start_date": "20200115"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (16571-660-50)", "package_ndc": "16571-660-50", "marketing_start_date": "20200115"}], "brand_name": "Meclizine Hydrochloride", "product_id": "16571-660_2be27ea6-3d0a-4036-ab42-fea4720daa34", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "16571-660", "generic_name": "Meclizine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Meclizine Hydrochloride", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "NDA010721", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200115", "listing_expiration_date": "20261231"}