Prednisone
- Product NDC
- 42291-771
- 11-digit product format
- 422910771
- Labeler code
- 42291
- Product ID
- 42291-771_d5c99427-ea8f-47d7-e053-2a95a90a9384
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA211575
- Marketing category
- ANDA
- Marketing start
- 2020-04-22
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-771-01 | 42291077101 | 100 TABLET in 1 BOTTLE (42291-771-01) | 100 tablet | 2020-04-22 | 0000-00-00 | No | No | Current |
| 42291-771-50 | 42291077150 | 500 TABLET in 1 BOTTLE (42291-771-50) | 500 tablet | 2020-04-22 | 0000-00-00 | No | No | Current |