NDC 68788-4056
Azelastine Hydrochloride 137 ug spray, metered
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Apotex Corp.'s NDC 60505-0833.
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.
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Recalls
- Jun 15, 2011 · Class III · Apotex Corp.
CGMP Deviations: tubing used for filling may interact with the nasal formulation of this product.
Lots: Lot #: JK9130, JM0925, Exp 05/12; JN6514, Exp 07/12; JN1125, JN1127, Exp 08/12; JR5780, JR5782, Exp 12/12.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Azelastine: every company that makes it
- Form
- spray, metered, nasal
- Strength
- 137 ug
- Approval
- ANDA ANDA077954
- On the market since
- Nov 17, 2025
- Package NDCs
68788-4056-2- Official label
- DailyMed (National Library of Medicine), updated Nov 17, 2025
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