Prednisone
- Product NDC
- 70934-259
- 11-digit product format
- 709340259
- Labeler code
- 70934
- Product ID
- 70934-259_b556a4eb-af72-19b7-e053-2a95a90a584e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA085162
- Marketing category
- ANDA
- Marketing start
- 2019-01-25
- 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 |
|---|
| 70934-259-21 | 70934025921 | 21 TABLET in 1 BOTTLE, PLASTIC (70934-259-21) | 21 tablet | 2019-01-25 | 0000-00-00 | No | No | Current |
| 70934-259-30 | 70934025930 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-259-30) | 30 tablet | 2019-02-04 | 0000-00-00 | No | No | Current |
| 70934-259-42 | 70934025942 | 42 TABLET in 1 BOTTLE, PLASTIC (70934-259-42) | 42 tablet | 2019-04-17 | 0000-00-00 | No | No | Current |