Methylprednisolone
- Product NDC
- 62135-762
- 11-digit product format
- 621350762
- Labeler code
- 62135
- Product ID
- 62135-762_225669c1-9479-52eb-e063-6394a90a649b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA209097
- Marketing category
- ANDA
- Marketing start
- 2019-02-22
- Substance
- METHYLPREDNISOLONE
- Active strength
- 16 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 | 16 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X4W7ZR7023 |
| Rxcui | 197969, 197971, 197973, 259966, 328161 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-762-50 | Methylprednisolone | 50 in 1 BOTTLE | TABLET | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-762 | METHYLPREDNISOLONE TABLET [CHARTWELL RX, LLC] | 2 | Current NDC, 1 package rows | 20240919_bdd048bb-7e6c-45c7-b51a-075e83ca9f5b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-762-50 | 62135076250 | 50 TABLET in 1 BOTTLE (62135-762-50) | 50 tablet | 2024-05-14 | No | No | Current |