Methylprednisolone Acetate
- Product NDC
- 0703-0051
- 11-digit product format
- 007030051
- Labeler code
- 0703
- Product ID
- 0703-0051_322c6b28-132a-41e1-9b0e-ea50f615d24c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone Acetate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE
- Labeler
- Teva Parenteral Medicines, Inc.
- 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
- 2022-12-31
- 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 |
|---|
| 0703-0051-01 | 00703005101 | 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-0051-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2005-03-08 | 0000-00-00 | No | No | Current |
| 0703-0051-04 | 00703005104 | 25 VIAL, SINGLE-DOSE in 1 TRAY (0703-0051-04) > 1 mL in 1 VIAL, SINGLE-DOSE | 2005-03-08 | 0000-00-00 | No | No | Current |