NDC 0093-7516
fluticasone propionate and salmeterol 50 ug / 500 ug powder
On the label: Teva Pharmaceuticals USA, Inc..
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Product details
- Generic drug
- Fluticasone and Salmeterol: every company that makes it
- Form
- powder, respiratory (inhalation)
- Strength
- 50 ug / 500 ug
- Approval
- ANDA ANDA213948
- On the market since
- Mar 23, 2022
- Package NDCs
0093-7516-31- Official label
- DailyMed (National Library of Medicine), updated Sep 28, 2022
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