NDC 37808-724 – Loratadine and Pseudoephedrine Sulfate

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

Human Otc Drug

Product NDC37808-724

Product details

Brand name
Loratadine and Pseudoephedrine Sulfate
Generic name
Loratadine and pseudoephedrine sulfate
Labeler
HEB
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA076557
Marketed since
February 1, 2018
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 (1)

Package NDCDescriptionSince
37808-724-6910 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (37808-724-69)Feb 1, 2018

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