Allegra Allergy
- Product NDC
- 67751-173
- 11-digit product format
- 677510173
- Labeler code
- 67751
- Product ID
- 67751-173_3d30db81-64fd-681f-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FEXOFENADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Navajo Manufacturing Company Inc.
- Application
- NDA020872
- Marketing category
- NDA
- Marketing start
- 2016-09-23
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#