NDC 45802-122 – loratadine D

Loratadine 5 mg/1; Pseudoephedrine Sulfate 120 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Otc Drug

Product NDC45802-122

Product details

Brand name
loratadine D
Generic name
loratadine, Pseudoephedrine sulfate
Labeler
Padagis Israel Pharmaceuticals Ltd
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA076050
Marketed since
April 10, 2018
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for loratadine D →

Package NDC codes (3)

Package NDCDescriptionSince
45802-122-4610 BLISTER PACK in 1 CARTON (45802-122-46) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKApr 10, 2018
45802-122-6020 BLISTER PACK in 1 CARTON (45802-122-60) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKApr 10, 2018
45802-122-6530 BLISTER PACK in 1 CARTON (45802-122-65) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKApr 10, 2018

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