methylprednisolone
- Product NDC
- 68180-688
- 11-digit product format
- 681800688
- Labeler code
- 68180
- Product ID
- 68180-688_c71a649a-a46d-4e69-81b8-f65e77a4c48b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA209097
- Marketing category
- ANDA
- Marketing start
- 2020-03-01
- Marketing end
- 0000-00-00
- Substance
- METHYLPREDNISOLONE
- Active strength
- 16 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68180-688-08 | methylprednisolone | 50 in 1 BOTTLE | TABLET | 50 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68180-688 | METHYLPREDNISOLONE TABLET [LUPIN PHARMACEUTICALS, INC.] | 7 | Legacy NDC, 1 package rows | 20211209_c5cbcea1-2200-4fc0-a49a-35edd9434873.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 |
|---|
| 68180-688-08 | 68180068808 | 50 TABLET in 1 BOTTLE (68180-688-08) | 50 tablet | 2020-03-01 | 0000-00-00 | No | No | Current |