Cetirizine Hydrochloride
- Product NDC
- 63629-2521
- 11-digit product format
- 636292521
- Labeler code
- 63629
- Product ID
- 63629-2521_67d9b612-788b-46fa-9625-c9b3a7ad9b66
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cetirizine hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078398
- Marketing category
- ANDA
- Marketing start
- 2008-07-24
- 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
- 2023-12-31
- 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 |
|---|
| 63629-2521-1 | 63629252101 | 1 BOTTLE in 1 CARTON (63629-2521-1) > 120 mL in 1 BOTTLE | 1 bottle | 2008-07-24 | 0000-00-00 | No | No | Current |