PREDNISONE
- Product NDC
- 60760-715
- 11-digit product format
- 607600715
- Labeler code
- 60760
- Product ID
- 60760-715_c6b490b9-bbc2-7109-e053-2a95a90a8e1a
- 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
- 2020-08-25
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 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 |
|---|
| 60760-715 | PREDNISONE TABLET [ST. MARY'S MEDICAL PARK PHARMACY] | 2 | Legacy NDC | 20210710_adb9ff9f-174f-0969-e053-2a95a90a3153.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-715-12 | 60760071512 | 12 TABLET in 1 BOTTLE, PLASTIC (60760-715-12) | 12 tablet | 2021-07-06 | 0000-00-00 | No | No | Current |
| 60760-715-21 | 60760071521 | 21 TABLET in 1 BOTTLE, PLASTIC (60760-715-21) | 21 tablet | 2020-08-25 | 0000-00-00 | No | No | Current |