Prednisone
- Product NDC
- 60760-002
- 11-digit product format
- 607600002
- Labeler code
- 60760
- Product ID
- 60760-002_ef5421f8-d69b-a805-e053-2995a90af843
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA040362
- Marketing category
- ANDA
- Marketing start
- 2015-11-13
- 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 |
|---|
| 60760-002-21 | 60760000221 | 21 TABLET in 1 BOTTLE (60760-002-21) | 21 tablet | 2015-12-04 | 0000-00-00 | No | No | Current |
| 60760-002-30 | 60760000230 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-002-30) | 30 tablet | 2015-11-13 | 0000-00-00 | No | No | Current |