Prednisone
- Product NDC
- 70934-218
- 11-digit product format
- 709340218
- Labeler code
- 70934
- Product ID
- 70934-218_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
- ANDA085161
- Marketing category
- ANDA
- Marketing start
- 2018-12-19
- 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
- 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 |
|---|
| 70934-218-10 | 70934021810 | 10 TABLET in 1 BOTTLE, PLASTIC (70934-218-10) | 10 tablet | 2020-04-09 | 0000-00-00 | No | No | Current |
| 70934-218-15 | 70934021815 | 15 TABLET in 1 BOTTLE, PLASTIC (70934-218-15) | 15 tablet | 2019-06-28 | 0000-00-00 | No | No | Current |
| 70934-218-20 | 70934021820 | 20 TABLET in 1 BOTTLE, PLASTIC (70934-218-20) | 20 tablet | 2019-01-15 | 0000-00-00 | No | No | Current |
| 70934-218-21 | 70934021821 | 21 TABLET in 1 BOTTLE, PLASTIC (70934-218-21) | 21 tablet | 2018-12-19 | 0000-00-00 | No | No | Current |
| 70934-218-30 | 70934021830 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-218-30) | 30 tablet | 2020-11-04 | 0000-00-00 | No | No | Current |