NDC 68382-917 – Methylprednisolone

Methylprednisolone 8 mg/1 · Tablet · Oral

Human Prescription Drug 5 recalls

Product NDC68382-917

Product details

Brand name
Methylprednisolone
Generic name
Methylprednisolone
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206751
Marketed since
May 1, 2018
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Methylprednisolone →

Package NDC codes (4)

Package NDCDescriptionSince
68382-917-01100 TABLET in 1 BOTTLE (68382-917-01)May 1, 2018
68382-917-05500 TABLET in 1 BOTTLE (68382-917-05)May 1, 2018
68382-917-1125 TABLET in 1 BOTTLE (68382-917-11)May 1, 2018
68382-917-7710 BLISTER PACK in 1 CARTON (68382-917-77) / 10 TABLET in 1 BLISTER PACK (68382-917-30)May 1, 2018

Recalls mentioning this NDC

Other Methylprednisolone products