Fexofenadine HCl
- Product NDC
- 11822-7663
- 11-digit product format
- 118227663
- Labeler code
- 11822
- Product ID
- 11822-7663_46553a37-c7d7-ba5b-e063-6394a90a584c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rite Aid
- Application
- ANDA211075
- Marketing category
- ANDA
- Marketing start
- 2024-10-25
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fexofenadine HCl
- Listing expiration
- 2027-12-31
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 |
|---|
| 11822-7663-4 | Fexofenadine HCl | 70 in 1 BOTTLE | TABLET | 70 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-7663 | FEXOFENADINE HCL TABLET [RITE AID] | 2 | Current NDC, 1 package rows | 20241226_1ddad045-7706-ea7e-e063-6394a90a2a5a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 11822-7663-4 | 11822766304 | 70 TABLET in 1 BOTTLE (11822-7663-4) | 70 tablet | 2024-10-25 | No | No | Current |