Prednisone
- Product NDC
- 70518-2314
- 11-digit product format
- 705182314
- Labeler code
- 70518
- Product ID
- 70518-2314_db5dbd25-9ddb-a896-e053-2a95a90ab1c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA085161
- Marketing category
- ANDA
- Marketing start
- 2019-09-16
- 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 |
|---|
| 70518-2314-0 | 70518231400 | 10 TABLET in 1 BOTTLE, PLASTIC (70518-2314-0) | 10 tablet | 2019-09-16 | 0000-00-00 | No | No | Current |
| 70518-2314-1 | 70518231401 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-2314-1) | 30 tablet | 2019-10-20 | 0000-00-00 | No | No | Current |
| 70518-2314-2 | 70518231402 | 14 TABLET in 1 BOTTLE, PLASTIC (70518-2314-2) | 14 tablet | 2020-05-19 | 0000-00-00 | No | No | Current |