NDC 71921-164
Doxepin Hydrochloride 50 mg capsule
On the label: Florida Pharmaceutical Products, LLC..
Where it's made
This label doesn't name the factory that makes the drug. 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 Florida Pharmaceutical Products, LLC. names for other drugs.
Product details
- Generic drug
- Doxepin: every company that makes it
- Form
- capsule, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA213474
- On the market since
- May 1, 2021
- Package NDCs
71921-164-01- Official label
- DailyMed (National Library of Medicine), updated Sep 24, 2021
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