PREDNISONE
- Product NDC
- 71329-104
- 11-digit product format
- 713290104
- Labeler code
- 71329
- Product ID
- 71329-104_c3dd4f62-cc06-4576-938c-c50f5a4a1642
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- GeneYork Pharmaceuticals Group LLC
- 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 [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71329-104-01 | 71329010401 | 1 BOTTLE, PLASTIC in 1 CARTON (71329-104-01) > 500 TABLET in 1 BOTTLE, PLASTIC | 2018-12-04 | 0000-00-00 | No | No | Current |
| 71329-104-02 | 71329010402 | 1 BOTTLE, PLASTIC in 1 CARTON (71329-104-02) > 100 TABLET in 1 BOTTLE, PLASTIC | 2018-12-04 | 0000-00-00 | No | No | Current |