NDC directory

FAMOTIDINE

NorthStar Rx LLC · POWDER, FOR SUSPENSION

72603-564ANDAHistamine H2 Receptor Antagonists [MoA]
Product NDC
72603-564
Generic name
FAMOTIDINE
Labeler name
NorthStar Rx LLC
Brand name
FAMOTIDINE
Finished
true
Listing expiration date
20271231
Marketing category
ANDA
Dosage form
POWDER, FOR SUSPENSION
SPL ID
4af90b5d-f47a-4436-8e24-4cb7e5b758b3
Product type
HUMAN PRESCRIPTION DRUG
Marketing start date
20261001
Product ID
72603-564_4af90b5d-f47a-4436-8e24-4cb7e5b758b3
Application number
ANDA219091
Brand name base
FAMOTIDINE
Active ingredients
  1. Name
    FAMOTIDINE
    Strength
    40 mg/5mL
Packaging
  1. Package NDC
    72603-564-01
    Description
    50 mL in 1 BOTTLE (72603-564-01)
    Marketing start date
    20261001
    Sample
    false
Route
ORAL
Pharm class
Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
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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.