Methylprednisolone Acetate
- Product NDC
- 63187-474
- 11-digit product format
- 631870474
- Labeler code
- 63187
- Product ID
- 63187-474_c2966446-a03f-4cd9-812e-a9861fc22b3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone Acetate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE
- Labeler
- Proficient Rx LP
- Application
- ANDA040557
- Marketing category
- ANDA
- Marketing start
- 2005-03-08
- Marketing end
- 0000-00-00
- Substance
- METHYLPREDNISOLONE ACETATE
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-474 | METHYLPREDNISOLONE ACETATE INJECTION, SUSPENSION [PROFICIENT RX LP] | 5 | Legacy NDC | 20200219_397cad9e-ab18-4271-8a17-9387c2358c49.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-474-01 | 63187047401 | 1 VIAL, SINGLE-DOSE in 1 CARTON (63187-474-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2015-02-02 | 0000-00-00 | No | No | Current |