NDC 69339-194 – Desloratadine

Desloratadine 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC69339-194

Product details

Brand name
Desloratadine
Generic name
Desloratadine
Labeler
Natco Pharma USA LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078351
Marketed since
April 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Histamine-1 Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Desloratadine →

Package NDC codes (2)

Package NDCDescriptionSince
69339-194-01100 TABLET, FILM COATED in 1 BOTTLE (69339-194-01)Apr 1, 2026
69339-194-05500 TABLET, FILM COATED in 1 BOTTLE (69339-194-05)Apr 1, 2026

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