Cetirizine Hydrochloride
- Product NDC
- 50090-2084
- 11-digit product format
- 500902084
- Labeler code
- 50090
- Product ID
- 50090-2084_9a00f78c-9808-451e-a21e-cd4b5b34d286
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2084-0 | 50090208400 | 120 mL in 1 BOTTLE, GLASS (50090-2084-0) | 120 ml | 2015-10-08 | 0000-00-00 | No | No | Current |