Prednisone
- Product NDC
- 70518-0307
- 11-digit product format
- 705180307
- Labeler code
- 70518
- Product ID
- 70518-0307_e761d629-b379-357f-e053-2995a90a1e9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040256
- Marketing category
- ANDA
- Marketing start
- 2017-03-10
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 10 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
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0307 | PREDNISONE TABLET [REMEDYREPACK INC.] | 14 | Legacy NDC | 20250425_027a8d36-d58f-4a3f-b456-0b6859e26d6b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0307-0 | 70518030700 | 21 TABLET in 1 BOX, UNIT-DOSE (70518-0307-0) | 21 tablet | 2017-03-10 | 0000-00-00 | No | No | Current |