NDC 68788-8605 – Loratadine

Loratadine 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC68788-8605

Product details

Brand name
Loratadine
Generic name
Loratadine
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211718
Marketed since
March 13, 2024
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Loratadine →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8605-010 TABLET in 1 BOTTLE (68788-8605-0)Mar 13, 2024
68788-8605-114 TABLET in 1 BOTTLE (68788-8605-1)Mar 13, 2024
68788-8605-330 TABLET in 1 BOTTLE (68788-8605-3)Mar 13, 2024
68788-8605-515 TABLET in 1 BOTTLE (68788-8605-5)Mar 13, 2024
68788-8605-990 TABLET in 1 BOTTLE (68788-8605-9)Mar 13, 2024

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