Levocetirizine Dihydrochloride
- Product NDC
- 71205-476
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levocetirizine Dihydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA203646
- Marketing category
- ANDA
- Substance
- LEVOCETIRIZINE DIHYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-476-30 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-476-30) | 2020-09-23 | | No | Historical |
| 71205-476-60 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-476-60) | 2020-09-23 | | No | Historical |
| 71205-476-90 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-476-90) | 2020-09-23 | | No | Historical |