METHYLPREDNISOLONE
- Product NDC
- 72189-264
- 11-digit product format
- 721890264
- Labeler code
- 72189
- Product ID
- 72189-264_2c28f93c-99a2-f643-e063-6394a90a6f9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHYLPREDNISOLONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA204072
- Marketing category
- ANDA
- Marketing start
- 2021-09-13
- 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, 762675 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-264-21 | METHYLPREDNISOLONE | 21 in 1 BOTTLE | TABLET | 21 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-264 | METHYLPRED DP TABLET METHYLPREDNISOLONE TABLET [DIRECT_RX] | 2 | Current NDC, Legacy NDC, 1 package rows | 20210915_8c3f3f63-8a05-7a4a-e053-2995a90ad95a.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 |
|---|
| 72189-264-21 | 72189026421 | 21 TABLET in 1 BOTTLE (72189-264-21) | 21 tablet | 2021-09-13 | 0000-00-00 | No | No | Current |