Levocetirizine Dihydrochloride
- Product NDC
- 71335-1405
- 11-digit product format
- 713351405
- Labeler code
- 71335
- Product ID
- 71335-1405_d732702f-8f97-41fe-a9b1-f4f8360306a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levocetirizine Dihydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1405-1 | 71335140501 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1405-1) | 2019-11-19 | 0000-00-00 | No | No | Current |
| 71335-1405-2 | 71335140502 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1405-2) | 2019-11-19 | 0000-00-00 | No | No | Current |
| 71335-1405-3 | 71335140503 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-1405-3) | 2019-11-19 | 0000-00-00 | No | No | Current |
| 71335-1405-4 | 71335140504 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1405-4) | 2019-11-19 | 0000-00-00 | No | No | Current |