Cetirizine Hydrochloride
- Product NDC
- 68151-3708
- 11-digit product format
- 681513708
- Labeler code
- 68151
- Product ID
- 68151-3708_223f78f6-626e-4bfe-a9b5-a6a139b46e00
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA078488
- Marketing category
- ANDA
- Marketing start
- 2013-12-03
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-3708-1 | Cetirizine Hydrochloride | 1 mL in 1 SYRINGE, PLASTIC | SOLUTION | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-3708 | CETIRIZINE HYDROCHLORIDE SOLUTION [CARILION MATERIALS MANAGEMENT] | 2 | Legacy NDC, 1 package rows | 20171229_b6c435bb-0a4f-422d-814d-a95db5404e87.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 68151-3708-1 | 68151370801 | 1 mL in 1 SYRINGE, PLASTIC | 1 ml | Historical |