Allergy Relief
- Product NDC
- 21130-064
- 11-digit product format
- 211300064
- Labeler code
- 21130
- Product ID
- 21130-064_b58f28e7-1e84-4bb8-ba3f-15b87647d3d1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Safeway, Inc.
- Application
- ANDA204097
- Marketing category
- ANDA
- Marketing start
- 2019-10-01
- Marketing end
- 2025-02-28
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21130-064-15 | 21130006415 | 15 BLISTER PACK in 1 CARTON (21130-064-15) > 1 TABLET, COATED in 1 BLISTER PACK | 15 blister pack | 2019-10-01 | 2025-02-28 | No | No | Current |
| 21130-064-30 | 21130006430 | 1 BOTTLE, PLASTIC in 1 BOX (21130-064-30) > 30 TABLET, COATED in 1 BOTTLE, PLASTIC | | 2019-10-01 | 2025-02-28 | No | No | Current |