NDC 68554-5063-4 - 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
- 68554-5063-4
- 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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.