PREDNISONE
- Product NDC
- 71205-460
- 11-digit product format
- 712050460
- Labeler code
- 71205
- Product ID
- 71205-460_cd05bda0-f38f-4ad8-ad0a-f81ed1871843
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA210525
- Marketing category
- ANDA
- Marketing start
- 2018-12-04
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 50 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-460 | PREDNISONE TABLET [PROFICIENT RX LP] | 3 | Legacy NDC | 20220421_989f644b-86fc-4bf4-b341-d6b7a4fa87ff.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-460-05 | 71205046005 | 5 TABLET in 1 BOTTLE, PLASTIC (71205-460-05) | 5 tablet | 2020-06-25 | 0000-00-00 | No | No | Current |
| 71205-460-07 | 71205046007 | 7 TABLET in 1 BOTTLE, PLASTIC (71205-460-07) | 7 tablet | 2020-06-25 | 0000-00-00 | No | No | Current |
| 71205-460-08 | 71205046008 | 8 TABLET in 1 BOTTLE, PLASTIC (71205-460-08) | 8 tablet | 2022-03-09 | 0000-00-00 | No | No | Current |
| 71205-460-30 | 71205046030 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-460-30) | 30 tablet | 2020-06-25 | 0000-00-00 | No | No | Current |
| 71205-460-60 | 71205046060 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-460-60) | 60 tablet | 2020-06-25 | 0000-00-00 | No | No | Current |
| 71205-460-90 | 71205046090 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-460-90) | 90 tablet | 2020-06-25 | 0000-00-00 | No | No | Current |