PredniSONE
- Product NDC
- 70934-307
- 11-digit product format
- 709340307
- Labeler code
- 70934
- Product ID
- 70934-307_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
- ANDA087342
- Marketing category
- ANDA
- Marketing start
- 2019-03-12
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 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 |
|---|
| 70934-307-10 | 70934030710 | 10 TABLET in 1 BOTTLE, PLASTIC (70934-307-10) | 10 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |
| 70934-307-15 | 70934030715 | 15 TABLET in 1 BOTTLE, PLASTIC (70934-307-15) | 15 tablet | 2019-03-12 | 0000-00-00 | No | No | Current |
| 70934-307-18 | 70934030718 | 18 TABLET in 1 BOTTLE, PLASTIC (70934-307-18) | 18 tablet | 2019-05-01 | 0000-00-00 | No | No | Current |
| 70934-307-20 | 70934030720 | 20 TABLET in 1 BOTTLE, PLASTIC (70934-307-20) | 20 tablet | 2019-04-30 | 0000-00-00 | No | No | Current |
| 70934-307-21 | 70934030721 | 21 TABLET in 1 BOTTLE, PLASTIC (70934-307-21) | 21 tablet | 2019-04-08 | 0000-00-00 | No | No | Current |
| 70934-307-30 | 70934030730 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-307-30) | 30 tablet | 2019-04-08 | 0000-00-00 | No | No | Current |