Prednisone
- Product NDC
- 71335-1294
- 11-digit product format
- 713351294
- Labeler code
- 71335
- Product ID
- 71335-1294_e7edfa40-0481-47f2-9c9b-313cb425c511
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA085161
- Marketing category
- ANDA
- Marketing start
- 1990-01-01
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 71335-1294-1 | 71335129401 | 14 TABLET in 1 BOTTLE (71335-1294-1) | 14 tablet | 2019-08-29 | 0000-00-00 | No | No | Current |
| 71335-1294-2 | 71335129402 | 10 TABLET in 1 BOTTLE (71335-1294-2) | 10 tablet | 2019-08-29 | 0000-00-00 | No | No | Current |
| 71335-1294-3 | 71335129403 | 18 TABLET in 1 BOTTLE (71335-1294-3) | 18 tablet | 2019-08-29 | 0000-00-00 | No | No | Current |
| 71335-1294-4 | 71335129404 | 20 TABLET in 1 BOTTLE (71335-1294-4) | 20 tablet | 2019-08-29 | 0000-00-00 | No | No | Current |