NDC directory

Losartan potassium

St. Mary's Medical Park Pharmacy · TABLET, FILM COATED

60760-876ANDAAngiotensin 2 Receptor Antagonists [MoA]
Product NDC
60760-876
Generic name
Losartan potassium
Labeler name
St. Mary's Medical Park Pharmacy
Brand name
Losartan potassium
Finished
true
Listing expiration date
20271231
Marketing category
ANDA
Dosage form
TABLET, FILM COATED
SPL ID
5f67878c-be27-db50-e063-6294a90ac95a
Product type
HUMAN PRESCRIPTION DRUG
Marketing start date
20261102
Product ID
60760-876_5f67878c-be27-db50-e063-6294a90ac95a
Application number
ANDA217396
Brand name base
Losartan potassium
Active ingredients
  1. Name
    LOSARTAN POTASSIUM
    Strength
    50 mg/1
Packaging
  1. Package NDC
    60760-876-30
    Description
    30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-876-30)
    Marketing start date
    20261102
    Sample
    false
Route
ORAL
Pharm class
Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [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.