Depo-Medrol
- Product NDC
- 0009-0274
- 11-digit product format
- 000090274
- Labeler code
- 0009
- Product ID
- 0009-0274_267dd735-f800-4735-ba1c-d39d00f0cee5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone acetate
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE
- Labeler
- Pharmacia & Upjohn Company LLC
- Application
- NDA011757
- Marketing category
- NDA
- Marketing start
- 1959-05-28
- Substance
- METHYLPREDNISOLONE ACETATE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Depo-Medrol
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHYLPREDNISOLONE ACETATE | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 43502P7F0P |
| Rxcui | 1358510, 1358512, 1358610, 1358612, 1358617, 1358619 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0009-0274-01 | Depo-Medrol | 5 mL in 1 VIAL, MULTI-DOSE | INJECTION, SUSPENSION | 5 | | 22 |
| 0009-0274-01 | Depo-Medrol | 1 in 1 CARTON | INJECTION, SUSPENSION | 1 | | 22 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| METHYLPREDNISOLONE ACETATE | ACTIVE INGREDIENT | 43502P7F0P | DEPO-MEDROL (METHYLPREDNISOLONE ACETATE) INJECTION, SUSPENSION [PHARMACIA AND UPJOHN COMPANY] | 6 | |
| METHYLPREDNISOLONE | ACTIVE MOIETY | X4W7ZR7023 | DEPO-MEDROL (METHYLPREDNISOLONE ACETATE) INJECTION, SUSPENSION [PHARMACIA AND UPJOHN COMPANY] | 6 | |
| BENZYL ALCOHOL | INACTIVE INGREDIENT | LKG8494WBH | DEPO-MEDROL (METHYLPREDNISOLONE ACETATE) INJECTION, SUSPENSION [PHARMACIA AND UPJOHN COMPANY] | 6 | |
| HYDROCHLORIC ACID | INACTIVE INGREDIENT | QTT17582CB | DEPO-MEDROL (METHYLPREDNISOLONE ACETATE) INJECTION, SUSPENSION [PHARMACIA AND UPJOHN COMPANY] | 6 | |
| POLYETHYLENE GLYCOL 3350 | INACTIVE INGREDIENT | G2M7P15E5P | DEPO-MEDROL (METHYLPREDNISOLONE ACETATE) INJECTION, SUSPENSION [PHARMACIA AND UPJOHN COMPANY] | 6 | |
| POLYSORBATE 80 | INACTIVE INGREDIENT | 6OZP39ZG8H | DEPO-MEDROL (METHYLPREDNISOLONE ACETATE) INJECTION, SUSPENSION [PHARMACIA AND UPJOHN COMPANY] | 6 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | DEPO-MEDROL (METHYLPREDNISOLONE ACETATE) INJECTION, SUSPENSION [PHARMACIA AND UPJOHN COMPANY] | 6 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | DEPO-MEDROL (METHYLPREDNISOLONE ACETATE) INJECTION, SUSPENSION [PHARMACIA AND UPJOHN COMPANY] | 6 | |
| SODIUM PHOSPHATE, DIBASIC | INACTIVE INGREDIENT | GR686LBA74 | DEPO-MEDROL (METHYLPREDNISOLONE ACETATE) INJECTION, SUSPENSION [PHARMACIA AND UPJOHN COMPANY] | 6 | |
| SODIUM PHOSPHATE, MONOBASIC | INACTIVE INGREDIENT | 3980JIH2SW | DEPO-MEDROL (METHYLPREDNISOLONE ACETATE) INJECTION, SUSPENSION [PHARMACIA AND UPJOHN COMPANY] | 6 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0009-0274 | DEPO-MEDROL (METHYLPREDNISOLONE ACETATE) INJECTION, SUSPENSION [PHARMACIA & UPJOHN COMPANY LLC] | 20 | Current NDC, Legacy NDC, 2 package rows | 20240618_823b0010-2b57-4e76-b5ac-4a8c2963438f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0009-0274-01 | 00009027401 | 1 VIAL, MULTI-DOSE in 1 CARTON (0009-0274-01) / 5 mL in 1 VIAL, MULTI-DOSE | 1959-05-28 | 0000-00-00 | No | No | Current |