NDC 68554-5063-3 - Fexofenadine Hydrochloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 68554-5063
- Requested NDC
- 68554-5063-3
- Package NDCs from labels
- 68554-5063-0, 68554-5063-1, 68554-5063-2, 68554-5063-4, 68554-5063-5, 68554-5063-3, 68554-5063-6
- Manufacturer
- Hetero Labs Limited
- Effective date
- 2016-09-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Fexofenadine Hydrochloride - Hetero Labs Limited | Hetero Labs Limited | 2016-09-08 | Human OTC Drug Label |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68554-5063-0 | Fexofenadine Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 2 | |
| 68554-5063-0 | Fexofenadine Hydrochloride | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 2 | |
| 68554-5063-1 | Fexofenadine Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 2 | |
| 68554-5063-1 | Fexofenadine Hydrochloride | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 2 | |
| 68554-5063-2 | Fexofenadine Hydrochloride | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 2 | |
| 68554-5063-2 | Fexofenadine Hydrochloride | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 2 | |
| 68554-5063-3 | Fexofenadine Hydrochloride | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 2 | |
| 68554-5063-4 | Fexofenadine Hydrochloride | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 2 | |
| 68554-5063-5 | Fexofenadine Hydrochloride | 7 in 1 CARTON | TABLET, FILM COATED | 7 | 2 | |
| 68554-5063-6 | Fexofenadine Hydrochloride | 15 in 1 CARTON | TABLET, FILM COATED | 15 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68554-5063 | FEXOFENADINE HYDROCHLORIDE TABLET, FILM COATED [HETERO LABS LIMITED] | 2 | Legacy NDC, 10 package rows | 20160909_412af925-12e9-405f-b3c3-d5c3d0b5d5c2.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.