Class II · Moderate risk
Fluticasone Propionate Nasal Spray USP 50mcg
CGMP Deviations: potential presence of Burkholderia cepacia complex
National Drug Code
Is NDC 60505-0829-01 recalled?
Fluticasone Propionate · 1 BOTTLE, SPRAY in 1 CARTON (60505-0829-1) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY
Yes — this exact package was recalled
3 FDA recalls name the code 60505-0829-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Fluticasone Propionate
- Strength
- FLUTICASONE PROPIONATE 50 ug/1
- Form
- Spray, Metered · Nasal
- Labeler
- Apotex Corp.
- Type
- Human Prescription Drug
- Product code
- 60505-0829
Recalls naming this package
Class II · Moderate risk
Fluticasone Propionate Nasal Spray USP
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Class II · Moderate risk
Fluticasone propionate Nasal Spray
Presence of foreign substance: glass particles
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 60505-0589 Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 3
- 60505-2580 Atorvastatin Calcium 3
- 60505-0595 See recall 2
- 60505-0596 See recall 2
- 60505-0773 See recall 2
- 60505-1003 Ketorolac Tromethamine 2
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