Methylprednisolone acetate
- Product NDC
- 50090-6024
- 11-digit product format
- 500906024
- Labeler code
- 50090
- Product ID
- 50090-6024_4f9802d9-3540-4c51-827d-c3ce5ff9e8ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone acetate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE
- Labeler
- A-S Medication Solutions
- Application
- ANDA210043
- Marketing category
- ANDA
- Marketing start
- 2019-05-20
- Substance
- METHYLPREDNISOLONE ACETATE
- Active strength
- 80 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 43502P7F0P | METHYLPREDNISOLONE ACETATE | 53-36-1 | METHYLPREDNISOLONE ACETATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6024-0 | 50090602400 | 1 VIAL, SINGLE-DOSE in 1 CARTON (50090-6024-0) / 1 mL in 1 VIAL, SINGLE-DOSE | 2022-06-27 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Methylprednisolone acetate | A-S Medication Solutions | 2024-06-03 | HUMAN PRESCRIPTION DRUG LABEL | 8 |