Levocetirizine Dihydrochloride
- Product NDC
- 0527-1917
- 11-digit product format
- 005271917
- Labeler code
- 0527
- Product ID
- 0527-1917_6c388935-62dd-4b6e-a478-df92f00b49ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levocetirizine Dihydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA204599
- Marketing category
- ANDA
- Marketing start
- 2017-05-15
- Marketing end
- 2023-05-31
- Substance
- LEVOCETIRIZINE DIHYDROCHLORIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0527-1917-69 | 00527191769 | 1 BOTTLE in 1 CARTON (0527-1917-69) > 148 mL in 1 BOTTLE | 1 bottle | 2017-05-15 | 0000-00-00 | No | No | Current |