Gentak
- Product NDC
- 50090-0251
- 11-digit product format
- 500900251
- Labeler code
- 50090
- Product ID
- 50090-0251_b1f78fc0-3098-4984-8868-906962e4c36a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gentamicin Sulfate
- Dosage form
- OINTMENT
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA064093
- Marketing category
- ANDA
- Marketing start
- 2006-05-08
- Marketing end
- 0000-00-00
- Substance
- GENTAMICIN SULFATE
- Active strength
- 3 mg/g
- Pharmacologic classes
- Aminoglycoside Antibacterial [EPC],Aminoglycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 50090-0251-0 | 50090025100 | 1 TUBE in 1 CARTON (50090-0251-0) > 3.5 g in 1 TUBE | 1 tube | 2016-06-29 | 0000-00-00 | No | No | Current |