NDC 61919-429
Cetirizine Hydrochloride 10 mg tablet
On the label: Direct Rx. It's repackaged from NDC 16571-402, made by Rising Pharma Holdings, Inc. (Cetirizine Hydrochloride). 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 repackages 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
- Cetirizine: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA077829
- On the market since
- Dec 22, 2016
- Package NDCs
61919-429-30- Official label
- DailyMed (National Library of Medicine), updated Jan 12, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?