Azelastine Hydrochloride
- Product NDC
- 68071-4359
- 11-digit product format
- 680714359
- Labeler code
- 68071
- Product ID
- 68071-4359_6857aded-5391-5dc1-e053-2a91aa0a744c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azelastine Hydrochloride
- Dosage form
- SOLUTION/ DROPS
- Route
- INTRAOCULAR
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA078738
- Marketing category
- ANDA
- Marketing start
- 2010-05-31
- Marketing end
- 0000-00-00
- Substance
- AZELASTINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record