Methylprednisolone Acetate
- Product NDC
- 50090-4758
- 11-digit product format
- 500904758
- Labeler code
- 50090
- Product ID
- 50090-4758_8b9a6185-e315-4698-9c06-4468cca51a38
- 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
- ANDA040557
- Marketing category
- ANDA
- Marketing start
- 2005-03-08
- Marketing end
- 0000-00-00
- Substance
- METHYLPREDNISOLONE ACETATE
- Active strength
- 80 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4758-0 | 50090475800 | 1 VIAL, SINGLE-DOSE in 1 CARTON (50090-4758-0) > 1 mL in 1 VIAL, SINGLE-DOSE | 2019-11-27 | 0000-00-00 | No | No | Current |