Methylprednisolone acetate
- Product NDC
- 70518-3071
- 11-digit product format
- 705183071
- Labeler code
- 70518
- Product ID
- 70518-3071_c0184885-870e-12ce-e053-2a95a90ac8cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone acetate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA210043
- Marketing category
- ANDA
- Marketing start
- 2021-04-15
- 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 |
|---|
| 70518-3071-0 | 70518307100 | 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-3071-0) > 1 mL in 1 VIAL, SINGLE-DOSE (70518-3071-1) | 2021-04-15 | 0000-00-00 | No | No | Current |