Cetirizine Hydrochloride
- Product NDC
- 55301-939
- 11-digit product format
- 553010939
- Labeler code
- 55301
- Product ID
- 55301-939_497df1ad-c032-474f-aae4-1235f7e6f6cd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Army & Air Force Exchange Service
- Application
- ANDA077498
- Marketing category
- ANDA
- Marketing start
- 2007-12-27
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- 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 |
|---|
| 55301-939-30 | Cetirizine Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 55301-939-56 | Cetirizine Hydrochloride | 5 in 1 BLISTER PACK | TABLET | 5 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55301-939 | CETIRIZINE HYDROCHLORIDE TABLET [ARMY & AIR FORCE EXCHANGE SERVICE] | 1 | Legacy NDC, 2 package rows | 20121016_691ba15f-d840-41c2-8172-8e85f8434cd3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55301-939-30 | 55301093930 | 30 in 1 BOTTLE | Historical |
| 55301-939-56 | 55301093956 | 5 in 1 BLISTER PACK | Historical |