NDC 63824-056 – Mucinex DM

Guaifenesin 600 mg/1; Dextromethorphan Hydrobromide 30 mg/1 · Tablet, Extended Release · Oral

Human Otc Drug 1 recall

Product NDC63824-056

Product details

Brand name
Mucinex DM
Generic name
Guaifenesin and Dextromethorphan Hydrobromide
Labeler
Reckitt Benckiser LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
NDA · NDA021620
Marketed since
June 26, 2012
Listing expires
December 31, 2027
Pharmacologic class
Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Mucinex DM →

Package NDC codes (7)

Package NDCDescriptionSince
63824-056-321 BLISTER PACK in 1 CARTON (63824-056-32) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 26, 2012
63824-056-342 BLISTER PACK in 1 CARTON (63824-056-34) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 26, 2012
63824-056-361 BLISTER PACK in 1 CARTON (63824-056-36) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 26, 2012
63824-056-693 BLISTER PACK in 1 CARTON (63824-056-69) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACKJun 26, 2012
63824-056-722 TABLET, EXTENDED RELEASE in 1 POUCH (63824-056-72)Jun 26, 2012
63824-056-7424 POUCH in 1 CARTON (63824-056-74) / 2 TABLET, EXTENDED RELEASE in 1 POUCH (63824-056-73)Jun 26, 2012
63824-056-802 BLISTER PACK in 1 CARTON (63824-056-80) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMay 1, 2024

Recalls mentioning this NDC

Other Mucinex DM products