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NDC 63629-8500-01 levocetirizine dihydrochloride 5 mg/1 Details
levocetirizine dihydrochloride 5 mg/1
levocetirizine dihydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is LEVOCETIRIZINE DIHYDROCHLORIDE.
MedlinePlus Drug Summary
Levocetirizine is used to relieve runny nose; sneezing; and redness, itching, and tearing of the eyes caused by hay fever, seasonal allergies, and allergies to other substances such as dust mites, animal dander, and mold. It is also used to treat symptoms of hives, including itching and rash. Levocetirizine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
Related Packages: 63629-8500-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Levocetirizine
Product Information
| NDC | 63629-8500 |
|---|---|
| Product ID | 63629-8500_cd6cb7eb-9e20-414c-98ff-cc7472d29dcb |
| Associated GPIs | 41550027100320 |
| GCN Sequence Number | 048920 |
| GCN Sequence Number Description | levocetirizine dihydrochloride TABLET 5 MG ORAL |
| HIC3 | Z2Q |
| HIC3 Description | ANTIHISTAMINES - 2ND GENERATION |
| GCN | 14901 |
| HICL Sequence Number | 022959 |
| HICL Sequence Number Description | LEVOCETIRIZINE DIHYDROCHLORIDE |
| Brand/Generic | Generic |
| Proprietary Name | levocetirizine dihydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | levocetirizine dihydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 5 |
| Active Ingredient Units | mg/1 |
| Substance Name | LEVOCETIRIZINE DIHYDROCHLORIDE |
| Labeler Name | Bryant Ranch Prepack |
| Pharmaceutical Class | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA203646 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 63629-8500-01 (63629850001)
| NDC Package Code | 63629-8500-1 |
|---|---|
| Billing NDC | 63629850001 |
| Package | 30 TABLET in 1 BOTTLE (63629-8500-1) |
| Marketing Start Date | 2021-05-18 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |