Levocetirizine Dihydrochloride
- Product NDC
- 66336-720
- 11-digit product format
- 663360720
- Labeler code
- 66336
- Product ID
- 66336-720_201a5bf4-905f-4a4f-856b-114f90dce681
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levocetirizine Dihydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Dispensing Solutions, Inc.
- Application
- ANDA090199
- Marketing category
- ANDA
- Marketing start
- 2011-09-06
- Marketing end
- 0000-00-00
- Substance
- LEVOCETIRIZINE DIHYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| SOD6A38AGA | LEVOCETIRIZINE DIHYDROCHLORIDE | 130018-87-0 | LEVOCETIRIZINE DIHYDROCHLORIDE |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levocetirizine Dihydrochloride | Dispensing Solutions, Inc. | PSS World Medical, Inc. | 2013-06-11 | HUMAN PRESCRIPTION DRUG LABEL | 1 |