NDC 43598-008 – Guaifenesin 600 mg

Guaifenesin 600 mg/1 · Tablet, Extended Release · Oral

Human Otc Drug

Product NDC43598-008

Product details

Brand name
Guaifenesin 600 mg
Generic name
Guaifenesin
Labeler
Dr. Reddy's Laboratories Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA215932
Marketed since
March 15, 2022
Listing expires
December 31, 2026
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin 600 mg →

Package NDC codes (2)

Package NDCDescriptionSince
43598-008-015 BLISTER PACK in 1 CARTON (43598-008-01) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (43598-008-20)Sep 1, 2022
43598-008-402 BLISTER PACK in 1 CARTON (43598-008-40) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (43598-008-20)Mar 15, 2022

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