NDC 68382-918 – Methylprednisolone
Methylprednisolone 16 mg/1 · Tablet · Oral
Product NDC68382-918
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
- Methylprednisolone 16 mg/1
Uses, dosage, side effects and warnings for Methylprednisolone →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68382-918-01 | 100 TABLET in 1 BOTTLE (68382-918-01) | May 1, 2018 |
| 68382-918-05 | 500 TABLET in 1 BOTTLE (68382-918-05) | May 1, 2018 |
| 68382-918-18 | 50 TABLET in 1 BOTTLE (68382-918-18) | May 1, 2018 |
| 68382-918-77 | 10 BLISTER PACK in 1 CARTON (68382-918-77) / 10 TABLET in 1 BLISTER PACK (68382-918-30) | May 1, 2018 |
Recalls mentioning this NDC
- D-1453-2019 Jun 26, 2019 · Class II
CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure. - D-1451-2019 Jun 26, 2019 · Class II
CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure. - D-1448-2019 Jun 26, 2019 · Class II
CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure. - D-1450-2019 Jun 26, 2019 · Class II
CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure. - D-1449-2019 Jun 26, 2019 · Class II
CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure.
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