NDC 68001-438 – Loratadine

Loratadine 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC68001-438

Product details

Brand name
Loratadine
Generic name
Loratadine
Labeler
BluePoint Laboratories
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208314
Marketed since
August 26, 2020
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Loratadine →

Package NDC codes (4)

Package NDCDescriptionSince
68001-438-001 BOTTLE in 1 CARTON (68001-438-00) / 100 TABLET in 1 BOTTLEAug 26, 2020
68001-438-041 BOTTLE in 1 CARTON (68001-438-04) / 30 TABLET in 1 BOTTLEAug 26, 2020
68001-438-9610 BLISTER PACK in 1 CARTON (68001-438-96) / 10 TABLET in 1 BLISTER PACK (68001-438-16)Aug 26, 2020
68001-438-971 BOTTLE in 1 CARTON (68001-438-97) / 300 TABLET in 1 BOTTLEAug 26, 2020

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