meclizine hydrochloride

Generic: meclizine hydrochloride

Labeler: pd-rx 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 pd-rx pharmaceuticals, inc.
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

meclizine hydrochloride 25 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-250
Product ID 72789-250_40ad376a-ff00-ce39-e063-6294a90a7174
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 72789250
Hyphenated Format 72789-250

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
  • 12 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (72789-250-12)
  • 20 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (72789-250-20)
  • 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (72789-250-30)
source: ndc

Packages (3)

72789-250-12 12 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (72789-250-12) 72789-250-20 20 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (72789-250-20) 72789-250-30 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (72789-250-30)

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": "40ad376a-ff00-ce39-e063-6294a90a7174", "openfda": {"unii": ["HDP7W44CIO"], "rxcui": ["995632"], "spl_set_id": ["a9ad5d27-306d-48ca-a10d-0a0415d08f05"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (72789-250-12)", "package_ndc": "72789-250-12", "marketing_start_date": "20220505"}, {"sample": false, "description": "20 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (72789-250-20)", "package_ndc": "72789-250-20", "marketing_start_date": "20220505"}, {"sample": false, "description": "30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (72789-250-30)", "package_ndc": "72789-250-30", "marketing_start_date": "20220505"}], "brand_name": "Meclizine Hydrochloride", "product_id": "72789-250_40ad376a-ff00-ce39-e063-6294a90a7174", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "72789-250", "generic_name": "Meclizine Hydrochloride", "labeler_name": "PD-Rx 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": "20261231"}