NDC 21130-526 – Loratadine

Loratadine 10 mg/1 · Tablet · Oral

Human Otc Drug

Product NDC21130-526

Product details

Brand name
Loratadine
Generic name
Loratadine
Labeler
SAFEWAY INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076134
Marketed since
June 6, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Loratadine →

Package NDC codes (5)

Package NDCDescriptionSince
21130-526-131 BOTTLE in 1 CARTON (21130-526-13) / 120 TABLET in 1 BOTTLEJun 6, 2009
21130-526-313 BLISTER PACK in 1 CARTON (21130-526-31) / 10 TABLET in 1 BLISTER PACKJun 6, 2009
21130-526-381 BOTTLE in 1 CARTON (21130-526-38) / 365 TABLET in 1 BOTTLEJun 6, 2009
21130-526-431 BOTTLE in 1 CARTON (21130-526-43) / 45 TABLET in 1 BOTTLEJun 6, 2009
21130-526-691 BLISTER PACK in 1 CARTON (21130-526-69) / 10 TABLET in 1 BLISTER PACKJun 6, 2009

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