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NDC 50436-0015-01 METHYLPREDNISOLONE 4 mg/1 Details

METHYLPREDNISOLONE 4 mg/1

METHYLPREDNISOLONE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Unit Dose Services. The primary component is METHYLPREDNISOLONE.

MedlinePlus Drug Summary

Methylprednisolone, a corticosteroid, is similar to a natural hormone produced by your adrenal glands. It is often used to replace this chemical when your body does not make enough of it. It relieves inflammation (swelling, heat, redness, and pain) and is used to treat certain forms of arthritis; skin, blood, kidney, eye, thyroid, and intestinal disorders (e.g., colitis); severe allergies; and asthma. Methylprednisolone is also used to treat certain types of cancer. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 50436-0015-01
Last Updated: 04/14/2024
MedLinePlus Full Drug Details: Methylprednisolone

Product Information

NDC	50436-0015
Product ID	50436-0015_26a41379-2c7c-4f7a-b953-2157aee9625b
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	METHYLPREDNISOLONE
Proprietary Name Suffix	n/a
Non-Proprietary Name	METHYLPREDNISOLONE
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	4
Active Ingredient Units	mg/1
Substance Name	METHYLPREDNISOLONE
Labeler Name	Unit Dose Services
Pharmaceutical Class	Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA204072
Listing Certified Through	2024-12-31

Package

NDC 50436-0015-01 (50436001501)

Pricing Information	N/A
NDC Package Code	50436-0015-1
Billing NDC	50436001501
Package	21 TABLET in 1 BOTTLE (50436-0015-1)
Marketing Start Date	2023-07-26
NDC Exclude Flag	N