Allergy Relief
- Product NDC
- 54257-170
- 11-digit product format
- 542570170
- Labeler code
- 54257
- Product ID
- 54257-170_0e12b912-5db1-bb3e-e063-6394a90aa446
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FEXOFENADINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Magno-Humphries, Inc.
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2021-03-25
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Allergy Relief
- 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 |
|---|
| 54257-170-02 | Allergy Relief | 100 in 1 BOTTLE | TABLET | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54257-170 | ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE) TABLET [MAGNO-HUMPHRIES, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240104_1f8a2f98-7eba-48df-9589-58587d67ae0e.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 |
|---|
| 54257-170-02 | 54257017002 | 100 TABLET in 1 BOTTLE (54257-170-02) | 100 tablet | 2021-03-25 | 0000-00-00 | No | No | Current |