NDC 11822-4260 – Guaifenesin

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

Human Otc Drug

Product NDC11822-4260

Product details

Brand name
Guaifenesin
Generic name
Guaifenesin
Labeler
RITE AID CORPORATION
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA210453
Marketed since
June 29, 2022
Listing expires
December 31, 2026
Pharmacologic class
Expectorant

Active ingredients

Uses, dosage, side effects and warnings for Guaifenesin →

Package NDC codes (3)

Package NDCDescriptionSince
11822-4260-11 BLISTER PACK in 1 CARTON (11822-4260-1) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 29, 2022
11822-4260-22 BLISTER PACK in 1 CARTON (11822-4260-2) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 29, 2022
11822-4260-33 BLISTER PACK in 1 CARTON (11822-4260-3) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 29, 2022

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