NDC 11523-4359 – Claritin

Loratadine 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC11523-4359

Product details

Brand name
Claritin
Generic name
Loratadine
Labeler
Bayer HealthCare LLC.
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA019658
Marketed since
April 12, 1993
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Claritin →

Package NDC codes (9)

Package NDCDescriptionSince
11523-4359-11 BOTTLE in 1 CARTON (11523-4359-1) / 40 TABLET in 1 BOTTLEApr 12, 1993
11523-4359-21 BOTTLE in 1 CARTON (11523-4359-2) / 100 TABLET in 1 BOTTLEApr 12, 1993
11523-4359-31 BOTTLE in 1 CARTON (11523-4359-3) / 90 TABLET in 1 BOTTLENov 1, 2017
11523-4359-41 BOTTLE in 1 CARTON (11523-4359-4) / 55 TABLET in 1 BOTTLEFeb 15, 2019
11523-4359-51 BOTTLE in 1 CARTON (11523-4359-5) / 85 TABLET in 1 BOTTLEFeb 15, 2019
11523-4359-61 BOTTLE in 1 CARTON (11523-4359-6) / 110 TABLET in 1 BOTTLEDec 1, 2019
11523-4359-71 BOTTLE in 1 BLISTER PACK (11523-4359-7) / 115 TABLET in 1 BOTTLEApr 12, 1993
11523-4359-82 BOTTLE in 1 BLISTER PACK (11523-4359-8) / 60 TABLET in 1 BOTTLEApr 12, 1993
11523-4359-91 BOTTLE in 1 CARTON (11523-4359-9) / 35 TABLET in 1 BOTTLEDec 1, 2019

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