NDC 49348-543 – Loratadine and Pseudoephedrine Sulfate

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

Human Otc Drug 1 recall

Product NDC49348-543

Product details

Brand name
Loratadine and Pseudoephedrine Sulfate
Generic name
Loratadine and Pseudoephedrine Sulfate
Labeler
STRATEGIC SOURCING SERVICES
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
49348-543-0110 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (49348-543-01)Nov 17, 2004
49348-543-5715 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (49348-543-57)Nov 17, 2004

Recalls mentioning this NDC

Other Loratadine and Pseudoephedrine Sulfate products