NDC directory

Meclizine Hydrochloride

Meclizine Hydrochloride · AMOL PHARMACEUTICALS PRIVATE LIMITED · TABLET

63189-027DRUG FOR FURTHER PROCESSINGBulk ingredient
Product NDC
63189-027
Generic name
Meclizine Hydrochloride
Labeler name
AMOL PHARMACEUTICALS PRIVATE LIMITED
Finished
false
Listing expiration date
20271231
Marketing category
DRUG FOR FURTHER PROCESSING
Dosage form
TABLET
SPL ID
4c9368b9-ca73-4a46-8097-771ec0517c21
Product type
DRUG FOR FURTHER PROCESSING
Marketing start date
20261001
Product ID
63189-027_4c9368b9-ca73-4a46-8097-771ec0517c21
Active ingredients
  1. Name
    MECLIZINE HYDROCHLORIDE
    Strength
    25 mg/1
Packaging
  1. Package NDC
    63189-027-20
    Description
    2 DRUM in 1 BOX (63189-027-20) / 1 BAG in 1 DRUM / 33334 TABLET in 1 BAG
    Marketing start date
    01-OCT-26
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.