Prednisone
- Product NDC
- 68788-7281
- 11-digit product format
- 687887281
- Labeler code
- 68788
- Product ID
- 68788-7281_ee51bd8a-d202-48f7-b18c-2ffe94a5e9ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA080356
- Marketing category
- ANDA
- Marketing start
- 2019-01-16
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 68788-7281-2 | 68788728102 | 1 BLISTER PACK in 1 CARTON (68788-7281-2) > 21 TABLET in 1 BLISTER PACK | 1 blister pack | 2019-01-16 | 0000-00-00 | No | No | Current |