Prednisone
- Product NDC
- 70518-2115
- 11-digit product format
- 705182115
- Labeler code
- 70518
- Product ID
- 70518-2115_c611b71b-17a3-b77b-e053-2995a90aa5d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA088832
- Marketing category
- ANDA
- Marketing start
- 2019-05-23
- 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 |
|---|
| 70518-2115-0 | 70518211500 | 30 TABLET in 1 BLISTER PACK (70518-2115-0) | 30 tablet | 2019-05-23 | 0000-00-00 | No | No | Current |
| 70518-2115-1 | 70518211501 | 21 TABLET in 1 BLISTER PACK (70518-2115-1) | 21 tablet | 2020-02-25 | 0000-00-00 | No | No | Current |
| 70518-2115-2 | 70518211502 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-2115-2) | 30 tablet | 2020-08-21 | 0000-00-00 | No | No | Current |