PredniSONE
- Product NDC
- 70934-365
- 11-digit product format
- 709340365
- Labeler code
- 70934
- Product ID
- 70934-365_9cc5a1e8-1599-7678-e053-2a95a90a3ee6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PredniSONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA087801
- Marketing category
- ANDA
- Marketing start
- 2019-05-13
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70934-365-30 | 70934036530 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-365-30) | 30 tablet | 2019-05-13 | 0000-00-00 | No | No | Current |