PREDNISONE
- Product NDC
- 70518-2676
- 11-digit product format
- 705182676
- Labeler code
- 70518
- Product ID
- 70518-2676_d6e4638f-3baf-1fcc-e053-2995a90aa753
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211495
- Marketing category
- ANDA
- Marketing start
- 2020-04-07
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 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
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 |
|---|
| 70518-2676-0 | 70518267600 | 30 TABLET in 1 BLISTER PACK (70518-2676-0) | 30 tablet | 2020-04-07 | 0000-00-00 | No | No | Current |
| 70518-2676-1 | 70518267601 | 180 TABLET in 1 BOTTLE, PLASTIC (70518-2676-1) | 180 tablet | 2020-09-22 | 0000-00-00 | No | No | Current |