Prednisone
- Product NDC
- 68071-4691
- 11-digit product format
- 680714691
- Labeler code
- 68071
- Product ID
- 68071-4691_d58edd1a-6145-3f61-e053-2995a90a2345
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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 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 |
|---|
| 68071-4691-1 | 68071469101 | 10 TABLET in 1 BOTTLE (68071-4691-1) | 10 tablet | 2019-01-03 | 0000-00-00 | No | No | Current |
| 68071-4691-4 | 68071469104 | 4 TABLET in 1 BOTTLE (68071-4691-4) | 4 tablet | 2019-01-03 | 0000-00-00 | No | No | Current |
| 68071-4691-6 | 68071469106 | 6 TABLET in 1 BOTTLE (68071-4691-6) | 6 tablet | 2019-01-03 | 0000-00-00 | No | No | Current |