Prednisone
- Product NDC
- 67296-0974
- 11-digit product format
- 672960974
- Labeler code
- 67296
- Product ID
- 67296-0974_d68437c4-1ffb-bd5e-e053-2a95a90adf12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA083677
- Marketing category
- ANDA
- Marketing start
- 2009-08-03
- Marketing end
- 2022-08-31
- Substance
- PREDNISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-0974-1 | 67296097401 | 10 TABLET in 1 BOTTLE (67296-0974-1) | 10 tablet | 2009-08-03 | 0000-00-00 | No | No | Current |
| 67296-0974-2 | 67296097402 | 20 TABLET in 1 BOTTLE (67296-0974-2) | 20 tablet | 2009-08-03 | 0000-00-00 | No | No | Current |
| 67296-0974-5 | 67296097405 | 15 TABLET in 1 BOTTLE (67296-0974-5) | 15 tablet | 2009-08-03 | 0000-00-00 | No | No | Current |