Prednisone
- Product NDC
- 53002-3092
- 11-digit product format
- 530023092
- Labeler code
- 53002
- Product ID
- 53002-3092_ad8402b4-3525-4851-8388-1f7a2e7f0d4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA085162
- Marketing category
- ANDA
- Marketing start
- 1990-01-01
- 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
- 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 |
|---|
| 53002-3092-0 | 53002309200 | 50 TABLET in 1 BOTTLE (53002-3092-0) | 50 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |
| 53002-3092-3 | 53002309203 | 26 TABLET in 1 BOTTLE (53002-3092-3) | 26 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |
| 53002-3092-4 | 53002309204 | 36 TABLET in 1 BOTTLE (53002-3092-4) | 36 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |