Allergy Relief
- Product NDC
- 59726-504
- 11-digit product format
- 597260504
- Labeler code
- 59726
- Product ID
- 59726-504_40402e5c-c6b4-4b62-8b8e-9f473d1e9311
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA079112
- Marketing category
- ANDA
- Marketing start
- 2016-03-31
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-504-03 | 59726050403 | 3 BLISTER PACK in 1 CARTON (59726-504-03) > 1 TABLET in 1 BLISTER PACK | 3 blister pack | 2016-03-31 | 0000-00-00 | No | No | Current |
| 59726-504-12 | 59726050412 | 1 BOTTLE, PLASTIC in 1 BOX (59726-504-12) > 120 TABLET in 1 BOTTLE, PLASTIC | | 2016-03-31 | 0000-00-00 | No | No | Current |
| 59726-504-30 | 59726050430 | 30 BLISTER PACK in 1 CARTON (59726-504-30) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2016-03-31 | 0000-00-00 | No | No | Current |