Flo-Pred
- Product NDC
- 51672-1338
- 11-digit product format
- 516721338
- Labeler code
- 51672
- Product ID
- 51672-1338_79fbfd7c-6b29-466c-8e65-015be1652aea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prednisolone Acetate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Taro Pharmaceuticals U.S.A., Inc.
- Application
- NDA022067
- Marketing category
- NDA
- Marketing start
- 2008-01-17
- Marketing end
- 0000-00-00
- Substance
- PREDNISOLONE ACETATE
- Active strength
- 17 mg/5mL
- 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 |
|---|
| 51672-1338-3 | 51672133803 | 1 BOTTLE in 1 CARTON (51672-1338-3) > 52 mL in 1 BOTTLE | 1 bottle | 2008-01-17 | 0000-00-00 | No | No | Current |
| 51672-1338-5 | 51672133805 | 1 BOTTLE in 1 CARTON (51672-1338-5) > 37 mL in 1 BOTTLE | 1 bottle | 2008-01-17 | 0000-00-00 | No | No | Current |
| 51672-1338-6 | 51672133806 | 1 BOTTLE in 1 CARTON (51672-1338-6) > 65 mL in 1 BOTTLE | 1 bottle | 2008-01-17 | 0000-00-00 | No | No | Current |