Childrens Allergy
- Product NDC
- 79903-249
- 11-digit product format
- 799030249
- Labeler code
- 79903
- Product ID
- 79903-249_5dcc6b17-e3f7-4524-a35e-21aa98e46167
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fexofenadine HCL
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- WALMART INC. (see also Equate)
- Application
- ANDA203330
- Marketing category
- ANDA
- Marketing start
- 2024-03-01
- Substance
- FEXOFENADINE HYDROCHLORIDE
- Active strength
- 30 mg/5mL
- 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
- Childrens Allergy
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FEXOFENADINE HYDROCHLORIDE | 30 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2S068B75ZU |
| Rxcui | 997491 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 79903-249-04 | Childrens Allergy | 118 mL in 1 BOTTLE, PLASTIC | SUSPENSION | 118 | | 2 |
| 79903-249-04 | Childrens Allergy | 1 in 1 BOX | SUSPENSION | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79903-249 | CHILDRENS ALLERGY (FEXOFENADINE HCL) SUSPENSION [WALMART INC. (SEE ALSO EQUATE)] | 2 | Current NDC, 2 package rows | 20240323_fb163eea-b2d2-4f52-9123-0bbe28baf757.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 79903-249-04 | 79903024904 | 1 BOTTLE, PLASTIC in 1 BOX (79903-249-04) / 118 mL in 1 BOTTLE, PLASTIC | 2024-03-01 | No | No | Current |