NDC 70121-1574 – Methylprednisolone acetate
Methylprednisolone Acetate 80 mg/mL · Injection, Suspension · Intra-articular, Intralesional, Intramuscular, Soft Tissue
Product NDC70121-1574
Product details
- Brand name
- Methylprednisolone acetate
- Generic name
- Methylprednisolone acetate
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Injection, Suspension
- Route
- Intra-articular, Intralesional, Intramuscular, Soft Tissue
- Marketing category
- ANDA · ANDA210043
- Marketed since
- May 20, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Corticosteroid
Active ingredients
- Methylprednisolone Acetate 80 mg/mL
Uses, dosage, side effects and warnings for Methylprednisolone acetate →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 70121-1574-1 | 1 VIAL, SINGLE-DOSE in 1 CARTON (70121-1574-1) / 1 mL in 1 VIAL, SINGLE-DOSE | May 20, 2019 |
| 70121-1574-5 | 25 VIAL, SINGLE-DOSE in 1 CARTON (70121-1574-5) / 1 mL in 1 VIAL, SINGLE-DOSE | May 20, 2019 |
Recalls mentioning this NDC
- D-0756-2023 May 31, 2023 · Class III
Labeling: Not Elsewhere Classified; A typographical error was observed in the NDC number on the preprinted Individual Folding Cartons (secondary packaging only). Incorrect NDC Number 70121-1573-1;…
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