Childrens
- Product NDC
- 49348-972
- 11-digit product format
- 493480972
- Labeler code
- 49348
- Product ID
- 49348-972_fa33ef6f-3f62-4ff7-a6e8-ef431f4f209d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- McKesson
- Application
- ANDA090182
- Marketing category
- ANDA
- Marketing start
- 2008-04-22
- 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 |
|---|
| 49348-972-34 | Childrens all day allergy | 120 mL in 1 BOTTLE | SOLUTION | 120 | | 1 |
| 49348-972-34 | Childrens all day allergy | 1 in 1 CARTON | SOLUTION | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49348-972 | CHILDRENS ALL DAY ALLERGY (CETIRIZINE HYDROCHLORIDE) SOLUTION [MCKESSON] | 1 | Legacy NDC, 2 package rows | 20121205_0bca5f76-db36-4256-99d5-1461bb6ae05c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 49348-972-34 | 49348097234 | 120 mL in 1 BOTTLE | 120 ml | Historical |