Fexofenadine Hydrochloride
- Product NDC
- 50594-769
- 11-digit product format
- 505940769
- Labeler code
- 50594
- Product ID
- 50594-769_ba16c18c-dff1-b574-e053-2a95a90aba2a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Big Lots Stores, Inc.
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2018-10-15
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50594-769-03 | Fexofenadine Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50594-769 | FEXOFENADINE HYDROCHLORIDE TABLET, FILM COATED [BIG LOTS STORES, INC.] | 3 | Legacy NDC, 1 package rows | 20210131_7cd4457b-a801-12a1-e053-2991aa0a4f0a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50594-769-03 | 50594076903 | 30 TABLET, FILM COATED in 1 BOTTLE (50594-769-03) | 2018-10-15 | 0000-00-00 | No | No | Current |