Prednisone
- Product NDC
- 70518-1561
- 11-digit product format
- 705181561
- Labeler code
- 70518
- Product ID
- 70518-1561_e56e562c-5861-9357-e053-2995a90a1e2e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA085161
- Marketing category
- ANDA
- Marketing start
- 2018-10-19
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70518-1561-0 | 70518156100 | 30 TABLET in 1 BLISTER PACK (70518-1561-0) | 30 tablet | 2018-10-19 | 0000-00-00 | No | No | Current |
| 70518-1561-1 | 70518156101 | 10 TABLET in 1 BOTTLE, PLASTIC (70518-1561-1) | 10 tablet | 2019-10-23 | 0000-00-00 | No | No | Current |