cetirizine hydrochloride
- Product NDC
- 0615-8240
- 11-digit product format
- 006158240
- Labeler code
- 0615
- Product ID
- 0615-8240_470d2dfc-f9df-4f37-8601-2315d854bdb1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA078336
- 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
- 2022-12-31
- 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 |
|---|
| 0615-8240-39 | 00615824039 | 30 TABLET in 1 BLISTER PACK (0615-8240-39) | 30 tablet | 2018-11-07 | 0000-00-00 | No | No | Current |