NDC 21130-724 – Loratadine and Pseudoephedrine Sulfate

Loratadine 10 mg/1; Pseudoephedrine Sulfate 240 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Otc Drug

Product NDC21130-724

Product details

Brand name
Loratadine and Pseudoephedrine Sulfate
Generic name
Loratadine and Pseudoephedrine Sulfate
Labeler
Safeway Inc.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA076557
Marketed since
November 17, 2004
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Loratadine and Pseudoephedrine Sulfate →

Package NDC codes (2)

Package NDCDescriptionSince
21130-724-1515 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (21130-724-15)Nov 17, 2004
21130-724-6910 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (21130-724-69)Nov 17, 2004

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