NDC 33342-109 – Risedronate Sodium

Risedronate Sodium 35 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC33342-109

Product details

Brand name
Risedronate Sodium
Generic name
Risedronate Sodium
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203533
Marketed since
December 9, 2015
Listing expires
December 31, 2027
Pharmacologic class
Bisphosphonate

Active ingredients

Uses, dosage, side effects and warnings for Risedronate Sodium →

Package NDC codes (2)

Package NDCDescriptionSince
33342-109-371 BLISTER PACK in 1 CARTON (33342-109-37) / 4 TABLET, FILM COATED in 1 BLISTER PACKDec 9, 2015
33342-109-503 BLISTER PACK in 1 CARTON (33342-109-50) / 4 TABLET, FILM COATED in 1 BLISTER PACKDec 9, 2015

Recalls mentioning this NDC

Other Risedronate Sodium products