Tobramycin
- Product NDC
- 0781-7171
- 11-digit product format
- 007817171
- Labeler code
- 0781
- Product ID
- 0781-7171_872e298a-ced7-46d0-8b55-7302faf49e65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tobramycin
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- NDA050753
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2014-07-09
- Marketing end
- 0000-00-00
- Substance
- TOBRAMYCIN
- Active strength
- 300 mg/5mL
- Pharmacologic classes
- Aminoglycoside Antibacterial [EPC],Aminoglycosides [CS]
- 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 |
|---|
| 0781-7171-56 | 00781717156 | 56 AMPULE in 1 CARTON (0781-7171-56) > 5 mL in 1 AMPULE (0781-7171-75) | 56 ampule | 2014-07-09 | 0000-00-00 | No | No | Current |