# Methylprednisolone

NDC: 68084-149
Generic name: Methylprednisolone
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20131203

FDA application: ANDA040183

## Active ingredients

- METHYLPREDNISOLONE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68084-149"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68084-149
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=97256c7e-5694-4148-926f-594b9d5c34f4