NDC 68788-8659 – Loratadine

Loratadine 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC68788-8659

Product details

Brand name
Loratadine
Generic name
Loratadine
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210722
Marketed since
May 13, 2024
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Loratadine →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8659-010 TABLET in 1 BOTTLE (68788-8659-0)May 13, 2024
68788-8659-114 TABLET in 1 BOTTLE (68788-8659-1)May 13, 2024
68788-8659-330 TABLET in 1 BOTTLE (68788-8659-3)May 13, 2024
68788-8659-515 TABLET in 1 BOTTLE (68788-8659-5)May 13, 2024
68788-8659-990 TABLET in 1 BOTTLE (68788-8659-9)May 13, 2024

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