Gentamicin is a Intramuscular; Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Fresenius Kabi Usa, Llc. The primary component is Gentamicin Sulfate.
| Product ID | 63323-173_4a9149ef-4409-482b-bd5e-f52a9fd1469a |
| NDC | 63323-173 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Gentamicin |
| Generic Name | Gentamicin |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAMUSCULAR; INTRAVENOUS |
| Marketing Start Date | 2004-11-29 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA062366 |
| Labeler Name | Fresenius Kabi USA, LLC |
| Substance Name | GENTAMICIN SULFATE |
| Active Ingredient Strength | 10 mg/mL |
| Pharm Classes | Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2024-12-31 |
| Marketing Start Date | 2004-11-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA062366 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2004-11-29 |
| Marketing Category | ANDA |
| Application Number | ANDA062366 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2004-11-29 |
| Marketing Category | ANDA |
| Application Number | ANDA062366 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2004-11-29 |
| Ingredient | Strength |
|---|---|
| GENTAMICIN SULFATE | 10 mg/mL |
| SPL SET ID: | 63413469-c676-48a3-a945-7d2489b535ef |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0143-9128 | Gentamicin | Gentamicin |
| 0143-9129 | Gentamicin | Gentamicin |
| 0404-9866 | Gentamicin | Gentamicin Sulfate |
| 51662-1508 | GENTAMICIN | GENTAMICIN |
| 52584-010 | Gentamicin | Gentamicin Sulfate |
| 63323-010 | Gentamicin | GENTAMICIN SULFATE |
| 63323-173 | Gentamicin | GENTAMICIN |