CHILDRENS CETIRIZINE HYDROCHLORIDE
- Product NDC
- 79903-406
- 11-digit product format
- 799030406
- Labeler code
- 79903
- Product ID
- 79903-406_97ddae8d-b4cb-462d-8a9a-950ee6a658c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- WALMART INC.
- Application
- ANDA213557
- Marketing category
- ANDA
- Marketing start
- 2026-01-14
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 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
- CHILDRENS CETIRIZINE HYDROCHLORIDE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CETIRIZINE HYDROCHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 64O047KTOA |
| Rxcui | 1011482 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 79903-406-10 | CHILDRENS CETIRIZINE HYDROCHLORIDE | 4 in 1 CARTON | TABLET, ORALLY DISINTEGRATING | 4 | | 2 |
| 79903-406-10 | CHILDRENS CETIRIZINE HYDROCHLORIDE | 6 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 6 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 79903-406-10 | 79903040610 | 4 BLISTER PACK in 1 CARTON (79903-406-10) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 4 blister pack | 2026-01-14 | No | No | Historical |