Fexofenadine hydrochloride
- Product NDC
- 68196-976
- 11-digit product format
- 681960976
- Labeler code
- 68196
- Product ID
- 68196-976_52d0f22a-fe82-4725-aba6-f95a44740285
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sam's West Inc
- Application
- ANDA202039
- Marketing category
- ANDA
- Marketing start
- 2015-01-15
- Marketing end
- 0000-00-00
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 68196-976-91 | Fexofenadine hydrochloride | 150 in 1 BOTTLE | TABLET, FILM COATED | 150 | | 2 |
| 68196-976-91 | Fexofenadine hydrochloride | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68196-976 | FEXOFENADINE HYDROCHLORIDE TABLET, FILM COATED [SAM'S WEST INC] | 2 | Legacy NDC, 2 package rows | 20190911_53d6c830-060b-4427-8acc-51a6c50f8a11.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68196-976-91 | 68196097691 | 1 BOTTLE in 1 CARTON (68196-976-91) > 150 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2015-01-15 | 0000-00-00 | No | No | Current |