PREDNISONE
- Product NDC
- 70934-647
- 11-digit product format
- 709340647
- Labeler code
- 70934
- Product ID
- 70934-647_aa906a59-3071-f175-e053-2a95a90ad746
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA211495
- Marketing category
- ANDA
- Marketing start
- 2020-04-01
- 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 |
|---|
| 70934-647-30 | 70934064730 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-647-30) | 30 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |