NDC 71205-449
Azelastine Hydrochloride 137 ug spray, metered
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP 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
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels 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
- Mar 1, 2010
- Package NDCs
71205-449-30- Official label
- DailyMed (National Library of Medicine), updated Oct 1, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?