Fexofenadine Hydrochloride
- Product NDC
- 68210-2210
- 11-digit product format
- 682102210
- Labeler code
- 68210
- Product ID
- 68210-2210_292e71ee-f44d-0821-e063-6394a90a4187
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- SPIRIT PHARMACEUTICALS LLC
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2020-03-17
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fexofenadine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FEXOFENADINE HYDROCHLORIDE | 180 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2S068B75ZU |
| Rxcui | 997420 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68210-2210-1 | Fexofenadine Hydrochloride | 100 in 1 PACKAGE | TABLET, FILM COATED | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68210-2210 | FEXOFENADINE HYDROCHLORIDE TABLET, FILM COATED [SPIRIT PHARMACEUTICALS LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241215_ae0f16f6-d07a-47e1-adb8-07803c6cfb13.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 |
|---|
| 68210-2210-1 | 68210221001 | 100 TABLET, FILM COATED in 1 PACKAGE (68210-2210-1) | 2020-03-17 | 0000-00-00 | No | No | Current |