Prednicarbate
- Product NDC
- 68682-880
- 11-digit product format
- 686820880
- Labeler code
- 68682
- Product ID
- 68682-880_1bff5aba-dcc3-4875-8a58-78b4e7647e14
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- emollient
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA020279
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1993-10-29
- Marketing end
- 0000-00-00
- Substance
- PREDNICARBATE
- Active strength
- 1 mg/g
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68682-880-60 | 68682088060 | 60 g in 1 TUBE (68682-880-60) | 60 g | 1993-10-29 | 0000-00-00 | No | No | Current |