Methylprednisolone Acetate
- Product NDC
- 70518-2894
- 11-digit product format
- 705182894
- Labeler code
- 70518
- Product ID
- 70518-2894_d7868893-7bb9-cdff-e053-2a95a90ad4f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone Acetate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040557
- Marketing category
- ANDA
- Marketing start
- 2020-09-22
- Marketing end
- 0000-00-00
- Substance
- METHYLPREDNISOLONE ACETATE
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2894-0 | 70518289400 | 1 VIAL, SINGLE-DOSE in 1 CARTON (70518-2894-0) > 1 mL in 1 VIAL, SINGLE-DOSE | 2020-09-22 | 0000-00-00 | No | No | Current |