Allergy Relief
- Product NDC
- 71626-502
- 11-digit product format
- 716260502
- Labeler code
- 71626
- Product ID
- 71626-502_da618c87-4310-4ca3-a534-f5142d518c35
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCL
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Medstone Pharma LLC
- Application
- ANDA204097
- Marketing category
- ANDA
- Marketing start
- 2019-10-01
- Marketing end
- 2025-01-31
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71626-502-01 | 71626050201 | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (71626-502-01) | 2019-10-01 | 0000-00-00 | No | No | Current |
| 71626-502-05 | 71626050205 | 500 TABLET, COATED in 1 BOTTLE, PLASTIC (71626-502-05) | 2019-10-01 | 0000-00-00 | No | No | Current |