NDC 0536-1333 – Guaifenesin D

Guaifenesin 600 mg/1; Pseudoephedrine Hydrochloride 60 mg/1 · Tablet, Extended Release · Oral

Human Otc Drug

Product NDC0536-1333

Product details

Brand name
Guaifenesin D
Generic name
Guaifenesin and Pseudoephedrine Hydrochloride
Labeler
RUGBY LABORATORIES, INC.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA212542
Marketed since
April 4, 2022
Marketing end
March 31, 2027
Pharmacologic class
Expectorant; alpha-Adrenergic Agonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0536-1333-211 BLISTER PACK in 1 CARTON (0536-1333-21) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACKApr 4, 2022
0536-1333-362 BLISTER PACK in 1 CARTON (0536-1333-36) / 18 TABLET, EXTENDED RELEASE in 1 BLISTER PACKApr 4, 2022

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