NDC 70518-1655
Fluticasone Propionate 50 ug spray, metered
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Apotex Corp.'s NDC 60505-0829.
Where the pills inside were 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 Apotex Corp. names for other drugs.
Recalls
- Feb 9, 2024 · Class II · Apotex Corp.
CGMP Deviations: potential presence of Burkholderia cepacia complex
Lots: Lot number # TX5274 Exp. 09/30/2026 - Jan 26, 2022 · Class II · Cardinal Healthcare
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Lots: Batch TE9159, TE8156 - May 31, 2018 · Class II · Apotex Inc.
Presence of foreign substance: glass particles
Lots: Lot: NJ4501 Exp. 07/2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fluticasone: every company that makes it
- Form
- spray, metered, nasal
- Strength
- 50 ug
- Approval
- ANDA ANDA077538
- On the market since
- Nov 9, 2018
- Package NDCs
70518-1655-0- Official label
- DailyMed (National Library of Medicine), updated Sep 24, 2026
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