PRED-G
- Product NDC
- 0023-0066
- 11-digit product format
- 000230066
- Labeler code
- 0023
- Product ID
- 0023-0066_05f7c3fc-cc93-49c4-8e82-16bd49d79d73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- gentamicin sulfate and prednisolone acetate
- Dosage form
- OINTMENT
- Route
- OPHTHALMIC
- Labeler
- Allergan, Inc.
- Application
- NDA050612
- Marketing category
- NDA
- Marketing start
- 1990-01-01
- Marketing end
- 0000-00-00
- Substance
- GENTAMICIN SULFATE; PREDNISOLONE ACETATE
- Active strength
- 3 mg/g; mg/g
- Pharmacologic classes
- Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0023-0066-04 | 00023006604 | 1 TUBE in 1 CARTON (0023-0066-04) > 3.5 g in 1 TUBE | 1 tube | 1990-01-01 | 0000-00-00 | No | No | Current |