Tobramycin
- Product NDC
- 17478-114
- 11-digit product format
- 174780114
- Labeler code
- 17478
- Product ID
- 17478-114_0e8315f5-35e7-4725-bde8-a9f7cdda508a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tobramycin Sulfate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Akorn
- Application
- ANDA205179
- Marketing category
- ANDA
- Marketing start
- 2014-09-16
- Marketing end
- 0000-00-00
- Substance
- TOBRAMYCIN SULFATE
- Active strength
- 40 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-114-02 | 17478011402 | 25 VIAL, MULTI-DOSE in 1 CARTON (17478-114-02) > 2 mL in 1 VIAL, MULTI-DOSE | 2014-09-16 | 0000-00-00 | No | No | Current |
| 17478-114-30 | 17478011430 | 1 VIAL, MULTI-DOSE in 1 CARTON (17478-114-30) > 30 mL in 1 VIAL, MULTI-DOSE | 2014-09-16 | 0000-00-00 | No | No | Current |