NDC 69842-335 – Guaifenesin

Guaifenesin 1200 mg/1 · Tablet, Extended Release · Oral

Human Otc Drug

Product NDC69842-335

Product details

Brand name
Guaifenesin
Generic name
Guaifenesin
Labeler
CVS PHARMACY, INC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA213420
Marketed since
March 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin →

Package NDC codes (3)

Package NDCDescriptionSince
69842-335-1614 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69842-335-16)Mar 1, 2021
69842-335-2828 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69842-335-28)Mar 1, 2021
69842-335-4242 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69842-335-42)Mar 1, 2021

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