NDC 51660-724 – Loratadine and Pseudoephedrine

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

Human Otc Drug

Product NDC51660-724

Product details

Brand name
Loratadine and Pseudoephedrine
Generic name
Loratadine and pseudoephedrine
Labeler
Ohm Laboratories Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA076557
Marketed since
November 17, 2004
Listing expires
December 31, 2027
Pharmacologic class
alpha-Adrenergic Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
51660-724-043 BLISTER PACK in 1 CARTON (51660-724-04) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACKNov 17, 2004
51660-724-151 BLISTER PACK in 1 CARTON (51660-724-15) / 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACKNov 17, 2004
51660-724-691 BLISTER PACK in 1 CARTON (51660-724-69) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKNov 17, 2004

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