Gentamicin Sulfate
- Product NDC
- 70518-1323
- 11-digit product format
- 705181323
- Labeler code
- 70518
- Product ID
- 70518-1323_e38ca312-4ba7-615d-e053-2995a90afad5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gentamicin Sulfate
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA062196
- Marketing category
- ANDA
- Marketing start
- 2018-07-26
- Marketing end
- 0000-00-00
- Substance
- GENTAMICIN SULFATE
- Active strength
- 3 mg/mL
- Pharmacologic classes
- Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS]
- 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 |
|---|
| 70518-1323-0 | 70518132300 | 5 mL in 1 BOTTLE, PLASTIC (70518-1323-0) | 5 ml | 2018-07-26 | 0000-00-00 | No | No | Current |