Prednisone
- Product NDC
- 63739-588
- 11-digit product format
- 637390588
- Labeler code
- 63739
- Product ID
- 63739-588_b4c8b2e4-0554-354c-e053-2995a90a2d4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA085161
- Marketing category
- ANDA
- Marketing start
- 1990-01-01
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-588-10 | 63739058810 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-588-10) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2014-06-30 | 0000-00-00 | No | No | Current |