azelastine hcl nasal
- Product NDC
- 63629-2519
- 11-digit product format
- 636292519
- Labeler code
- 63629
- Product ID
- 63629-2519_88fe69d1-6637-46f0-871d-83b84f16d801
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azelastine HCl
- Dosage form
- SPRAY
- Route
- NASAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202743
- Marketing category
- ANDA
- Marketing start
- 2014-05-09
- Marketing end
- 0000-00-00
- Substance
- AZELASTINE HYDROCHLORIDE
- Active strength
- 206 ug/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2519-1 | 63629251901 | 1 BOTTLE in 1 CARTON (63629-2519-1) > 200 SPRAY in 1 BOTTLE | 1 bottle | 2014-05-09 | 0000-00-00 | No | No | Current |