Cetirizine Hydrochloride
- Product NDC
- 0781-1683
- 11-digit product format
- 007811683
- Labeler code
- 0781
- Product ID
- 0781-1683_1f37dec7-beb5-4add-84de-b49b69766b3e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA077946
- Marketing category
- ANDA
- Marketing start
- 2007-12-27
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 0781-1683-01 | 00781168301 | 100 TABLET in 1 BOTTLE (0781-1683-01) | 100 tablet | 2007-12-27 | 0000-00-00 | No | No | Current |
| 0781-1683-64 | 00781168364 | 30 TABLET in 1 BOX, UNIT-DOSE (0781-1683-64) | 30 tablet | 2007-12-27 | 0000-00-00 | No | No | Current |