NDC 72789-347 – Loratadine antihistamine

Loratadine 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC72789-347

Product details

Brand name
Loratadine antihistamine
Generic name
Loratadine
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076301
Marketed since
October 15, 2008
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Loratadine →

Package NDC codes (5)

Package NDCDescriptionSince
72789-347-1414 TABLET in 1 BOTTLE, PLASTIC (72789-347-14)Dec 18, 2025
72789-347-2020 TABLET in 1 BOTTLE, PLASTIC (72789-347-20)May 16, 2024
72789-347-3030 TABLET in 1 BOTTLE, PLASTIC (72789-347-30)Aug 23, 2023
72789-347-87300 TABLET in 1 BOTTLE, PLASTIC (72789-347-87)Aug 23, 2023
72789-347-9090 TABLET in 1 BOTTLE, PLASTIC (72789-347-90)Aug 23, 2023

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