sunmark
- Product NDC
- 49348-326
- 11-digit product format
- 493480326
- Labeler code
- 49348
- Product ID
- 49348-326_4e3feada-e5dd-42f1-823e-7fdf4d47c845
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- McKesson
- Application
- ANDA090182
- Marketing category
- ANDA
- Marketing start
- 2011-09-08
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 5 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49348-326-34 | sunmark Childrens Cetirizine | 1 in 1 CARTON | SOLUTION | 1 | | 1 |
| 49348-326-34 | sunmark Childrens Cetirizine | 120 mL in 1 BOTTLE | SOLUTION | 120 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49348-326 | SUNMARK CHILDRENS CETIRIZINE (CETIRIZINE HYDROCHLORIDE) SOLUTION [MCKESSON] | 1 | Legacy NDC, 2 package rows | 20130131_56dbbe45-1165-4e4a-9a04-5079e866347e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 49348-326-34 | 49348032634 | 1 in 1 CARTON | Historical |