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Levocetirizine Dihydrochloride
Levocetirizine Dihydrochloride - 31722-551-90 - (Levocetirizine Dihydrochloride)
Drug Information of Levocetirizine Dihydrochloride
| Product NDC: | 31722-551 |
| Proprietary Name: | Levocetirizine Dihydrochloride |
| Non Proprietary Name: | Levocetirizine Dihydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; Levocetirizine Dihydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levocetirizine Dihydrochloride
| Product NDC: | 31722-551 |
| Labeler Name: | Camber Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091264 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120629 |
Package Information of Levocetirizine Dihydrochloride
| Package NDC: | 31722-551-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (31722-551-90) |
NDC Information of Levocetirizine Dihydrochloride
| NDC Code | 31722-551-90 |
| Proprietary Name | Levocetirizine Dihydrochloride |
| Package Description | 90 TABLET in 1 BOTTLE (31722-551-90) |
| Product NDC | 31722-551 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levocetirizine Dihydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120629 |
| Marketing Category Name | ANDA |
| Labeler Name | Camber Pharmaceuticals, Inc. |
| Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC] |
