MethylPREDNISolone
- Product NDC
- 63629-2218
- 11-digit product format
- 636292218
- Labeler code
- 63629
- Product ID
- 63629-2218_24f454f7-fece-4084-8926-c7e7c7fcbe81
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040183
- Marketing category
- ANDA
- Marketing start
- 1998-12-22
- Substance
- METHYLPREDNISOLONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MethylPREDNISolone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHYLPREDNISOLONE | 4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X4W7ZR7023 |
| Rxcui | 259966 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-2218-1 | MethylPREDNISolone | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 106 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-2218 | METHYLPREDNISOLONE TABLET [BRYANT RANCH PREPACK] | 106 | Current NDC, Legacy NDC, 1 package rows | 20240415_01f0126c-da22-4ac0-8755-3bc589602e6a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2218-1 | 63629221801 | 100 TABLET in 1 BOTTLE, PLASTIC (63629-2218-1) | 100 tablet | 1998-12-22 | 0000-00-00 | No | No | Current |