PREDNISONE
- Product NDC
- 60760-615
- 11-digit product format
- 607600615
- Labeler code
- 60760
- Product ID
- 60760-615_b403e752-6d49-128f-e053-2a95a90aa153
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA210525
- Marketing category
- ANDA
- Marketing start
- 2020-11-05
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-615 | PREDNISONE TABLET [ST. MARY'S MEDICAL PARK PHARMACY] | 1 | Legacy NDC | 20201117_b403e258-34d7-f69e-e053-2a95a90ac185.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-615-18 | 60760061518 | 18 TABLET in 1 BOTTLE, PLASTIC (60760-615-18) | 18 tablet | 2020-11-05 | 0000-00-00 | No | No | Current |