PREDNISONE
- Product NDC
- 68071-2209
- 11-digit product format
- 680712209
- Labeler code
- 68071
- Product ID
- 68071-2209_dee7d2dd-0ce7-5f42-e053-2a95a90ab8ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA210525
- Marketing category
- ANDA
- Marketing start
- 2018-12-04
- Marketing end
- 0000-00-00
- Substance
- PREDNISONE
- Active strength
- 20 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
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 |
|---|
| 68071-2209-1 | 68071220901 | 100 TABLET in 1 BOTTLE, PLASTIC (68071-2209-1) | 100 tablet | 2020-07-07 | 0000-00-00 | No | No | Current |
| 68071-2209-6 | 68071220906 | 6 TABLET in 1 BOTTLE, PLASTIC (68071-2209-6) | 6 tablet | 2020-07-07 | 0000-00-00 | No | No | Current |