Curist Hives Relief
- Product NDC
- 72559-028
- 11-digit product format
- 725590028
- Labeler code
- 72559
- Product ID
- 72559-028_4c259f31-d98c-4491-e063-6294a90a68cd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine Hydrochloride 180 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Little Pharma, Inc.
- Application
- ANDA204507
- Marketing category
- ANDA
- Marketing start
- 2023-09-07
- 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
- Curist Hives Relief
- 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 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72559-028-40 | Curist Hives Relief | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72559-028 | CURIST HIVES RELIEF (FEXOFENADINE HYDROCHLORIDE 180 MG) TABLET [LITTLE PHARMA, INC.] | 1 | Current NDC, 1 package rows | 20230910_04c75e93-b1f4-2546-e063-6394a90af0e1.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 |
|---|
| 72559-028-40 | 72559002840 | 60 TABLET in 1 BOTTLE (72559-028-40) | 60 tablet | 2023-09-07 | No | No | Historical |