NDC 71335-2529 – Loratadine

Loratadine 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC71335-2529

Product details

Brand name
Loratadine
Generic name
Loratadine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210722
Marketed since
January 1, 2020
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Loratadine →

Package NDC codes (9)

Package NDCDescriptionSince
71335-2529-120 TABLET in 1 BOTTLE (71335-2529-1)Feb 10, 2025
71335-2529-230 TABLET in 1 BOTTLE (71335-2529-2)Nov 22, 2024
71335-2529-360 TABLET in 1 BOTTLE (71335-2529-3)Jun 13, 2025
71335-2529-414 TABLET in 1 BOTTLE (71335-2529-4)Jun 13, 2025
71335-2529-510 TABLET in 1 BOTTLE (71335-2529-5)Jun 13, 2025
71335-2529-690 TABLET in 1 BOTTLE (71335-2529-6)Dec 16, 2024
71335-2529-728 TABLET in 1 BOTTLE (71335-2529-7)Jun 13, 2025
71335-2529-815 TABLET in 1 BOTTLE (71335-2529-8)Jun 13, 2025
71335-2529-9100 TABLET in 1 BOTTLE (71335-2529-9)Jun 13, 2025

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