Prednisone
- Product NDC
- 71335-1285
- 11-digit product format
- 713351285
- Labeler code
- 71335
- Product ID
- 71335-1285_8718bf00-0b5f-4dcd-bf86-f078936e4a36
- 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
- 2021-12-31
- 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 |
|---|
| 71335-1285-1 | 71335128501 | 6 TABLET in 1 BOTTLE (71335-1285-1) | 6 tablet | 1990-01-01 | 0000-00-00 | No | No | Current |
| 71335-1285-2 | 71335128502 | 14 TABLET in 1 BOTTLE (71335-1285-2) | 14 tablet | 1990-01-01 | 0000-00-00 | No | No | Current |
| 71335-1285-3 | 71335128503 | 5 TABLET in 1 BOTTLE (71335-1285-3) | 5 tablet | 1990-01-01 | 0000-00-00 | No | No | Current |
| 71335-1285-4 | 71335128504 | 10 TABLET in 1 BOTTLE (71335-1285-4) | 10 tablet | 2019-08-22 | 0000-00-00 | No | No | Current |
| 71335-1285-5 | 71335128505 | 8 TABLET in 1 BOTTLE (71335-1285-5) | 8 tablet | 2019-08-22 | 0000-00-00 | No | No | Current |
| 71335-1285-6 | 71335128506 | 7 TABLET in 1 BOTTLE (71335-1285-6) | 7 tablet | 2019-08-22 | 0000-00-00 | No | No | Current |