PREDNISONE
- Product NDC
- 60760-932
- 11-digit product format
- 607600932
- Labeler code
- 60760
- Product ID
- 60760-932_c8aa48bb-c7cf-290f-e053-2995a90a78d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA211495
- Marketing category
- ANDA
- Marketing start
- 2021-07-09
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 5 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-932 | PREDNISONE TABLET [ST. MARY'S MEDICAL PARK PHARMACY] | 1 | Legacy NDC | 20210804_c8aa3894-60e4-179a-e053-2995a90a02ff.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-932-21 | 60760093221 | 21 TABLET in 1 BOTTLE, PLASTIC (60760-932-21) | 21 tablet | 2021-07-09 | 0000-00-00 | No | No | Current |