Fexofenadine HCL
- Product NDC
- 70934-601
- 11-digit product format
- 709340601
- Labeler code
- 70934
- Product ID
- 70934-601_ab84a3d6-9f64-5e02-e053-2a95a90a743b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA204097
- Marketing category
- ANDA
- Marketing start
- 2020-03-02
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70934-601-30 | 70934060130 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-601-30) | 30 tablet | 2020-03-02 | 0000-00-00 | No | No | Current |