Prednisone
- Product NDC
- 70518-0473
- 11-digit product format
- 705180473
- Labeler code
- 70518
- Product ID
- 70518-0473_a4de235b-b531-6c6f-e053-2995a90af17d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA088832
- Marketing category
- ANDA
- Marketing start
- 2017-04-28
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0473-2 | 70518047302 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-0473-2) | 30 tablet | 2018-10-29 | 0000-00-00 | No | No | Current |
| 70518-0473-3 | 70518047303 | 48 TABLET in 1 BOTTLE, PLASTIC (70518-0473-3) | 48 tablet | 2019-09-03 | 0000-00-00 | No | No | Current |