NDC 85237-1630 – Claritin

Loratadine 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC85237-1630

Product details

Brand name
Claritin
Generic name
Loratadine
Labeler
Select Consumer Group
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075209
Marketed since
December 1, 2020
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Claritin →

Package NDC codes (3)

Package NDCDescriptionSince
85237-1630-11 BLISTER PACK in 1 CARTON (85237-1630-1) / 1 TABLET in 1 BLISTER PACKAug 18, 2025
85237-1630-320 POUCH in 1 BOX, UNIT-DOSE (85237-1630-3) / 1 TABLET in 1 POUCHDec 27, 2025
85237-1630-425 POUCH in 1 BOX, UNIT-DOSE (85237-1630-4) / 1 TABLET in 1 POUCHDec 27, 2025

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