NDC 70771-1351 – Methylprednisolone

Methylprednisolone 32 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70771-1351

Product details

Brand name
Methylprednisolone
Generic name
Methylprednisolone
Labeler
Zydus Lifesciences Limited
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
70771-1351-1100 TABLET in 1 BOTTLE (70771-1351-1)May 1, 2018
70771-1351-410 BLISTER PACK in 1 CARTON (70771-1351-4) / 10 TABLET in 1 BLISTER PACK (70771-1351-2)May 1, 2018
70771-1351-5500 TABLET in 1 BOTTLE (70771-1351-5)May 1, 2018
70771-1351-825 TABLET in 1 BOTTLE (70771-1351-8)May 1, 2018

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