NDC 61919-106
gentamicin sulfate 3 mg per 1 mL solution/ drops
On the label: Direct Rx. It's repackaged from NDC 60758-188, made by Pacific Pharma, Inc. (Gentamicin Sulfate). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Direct Rx names for other drugs.
Product details
- Generic drug
- Gentamicin: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 3 mg per 1 mL
- Approval
- ANDA ANDA062452
- On the market since
- Jan 1, 2014
- Package NDCs
61919-106-05- Official label
- DailyMed (National Library of Medicine), updated Jan 10, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?