NDC 50436-3988
Meclizine Hydrochloride 25 mg tablet
On the label: Unit Dose Services.
It's a repackaged product (source NDC 49884-035, which isn't on a current label).
Where it's made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it and relabels it). Companies aren't required to print it on the label. The manufacturer's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Unit Dose Services uses for other drugs.
Product details
- Generic drug
- Meclizine: see every company that makes it
- Form
- tablet
- Strength
- 25 mg
- Approval
- ANDA ANDA087128
- On the market since
- Jun 3, 1981
- Package NDCs
50436-3988-150436-3988-3- Official label
- DailyMed (National Library of Medicine), updated Nov 7, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?