PREDNISONE
- Product NDC
- 70518-3138
- 11-digit product format
- 705183138
- Labeler code
- 70518
- Product ID
- 70518-3138_cba54d03-42fc-5989-e053-2a95a90a5a24
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA210525
- Marketing category
- ANDA
- Marketing start
- 2021-07-01
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 10 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3138-0 | 70518313800 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-3138-0) | 30 tablet | 2021-07-01 | 0000-00-00 | No | No | Current |
| 70518-3138-1 | 70518313801 | 48 TABLET in 1 BOTTLE, PLASTIC (70518-3138-1) | 48 tablet | 2021-09-08 | 0000-00-00 | No | No | Current |