Cetirizine Hydrochloride
- Product NDC
- 0363-9899
- 11-digit product format
- 003639899
- Labeler code
- 0363
- Product ID
- 0363-9899_ba16adf1-6f4c-b473-e053-2a95a90a7219
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- WALGREEN CO.
- Application
- ANDA209274
- Marketing category
- ANDA
- Marketing start
- 2018-10-19
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 0363-9899-09 | Cetirizine Hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
| 0363-9899-15 | Cetirizine Hydrochloride | 150 in 1 BOTTLE | TABLET | 150 | | 3 |
| 0363-9899-70 | Cetirizine Hydrochloride | 70 in 1 BOTTLE | TABLET | 70 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-9899 | CETIRIZINE HYDROCHLORIDE TABLET [WALGREEN CO.] | 3 | Legacy NDC, 3 package rows | 20210131_71c50496-8bb9-1c94-e053-2995a90aaffa.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0363-9899-09 | 00363989909 | 90 TABLET in 1 BOTTLE (0363-9899-09) | 90 tablet | 2018-10-19 | 0000-00-00 | No | No | Current |
| 0363-9899-15 | 00363989915 | 150 TABLET in 1 BOTTLE (0363-9899-15) | 150 tablet | 2018-10-19 | 0000-00-00 | No | No | Current |
| 0363-9899-70 | 00363989970 | 70 TABLET in 1 BOTTLE (0363-9899-70) | 70 tablet | 2018-10-19 | 0000-00-00 | No | No | Current |