PREDNISONE
- Product NDC
- 71335-1736
- 11-digit product format
- 713351736
- Labeler code
- 71335
- Product ID
- 71335-1736_efdf7873-d2e1-4d14-a4d6-c2350e1ab6bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210525
- Marketing category
- ANDA
- Marketing start
- 2018-12-04
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71335-1736-1 | 71335173601 | 6 TABLET in 1 BOTTLE (71335-1736-1) | 6 tablet | 2020-12-04 | 0000-00-00 | No | No | Current |
| 71335-1736-2 | 71335173602 | 14 TABLET in 1 BOTTLE (71335-1736-2) | 14 tablet | 2020-12-04 | 0000-00-00 | No | No | Current |
| 71335-1736-3 | 71335173603 | 5 TABLET in 1 BOTTLE (71335-1736-3) | 5 tablet | 2020-12-04 | 0000-00-00 | No | No | Current |
| 71335-1736-4 | 71335173604 | 10 TABLET in 1 BOTTLE (71335-1736-4) | 10 tablet | 2020-12-04 | 0000-00-00 | No | No | Current |
| 71335-1736-5 | 71335173605 | 8 TABLET in 1 BOTTLE (71335-1736-5) | 8 tablet | 2020-12-04 | 0000-00-00 | No | No | Current |
| 71335-1736-6 | 71335173606 | 7 TABLET in 1 BOTTLE (71335-1736-6) | 7 tablet | 2020-12-04 | 0000-00-00 | No | No | Current |
| 71335-1736-7 | 71335173607 | 24 TABLET in 1 BOTTLE (71335-1736-7) | 24 tablet | 2022-04-20 | 0000-00-00 | No | No | Current |