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NDC 68788-8204-00 Cetirizine Hydrochloride (Allergy) 10 mg/1 Details
Cetirizine Hydrochloride (Allergy) 10 mg/1
Cetirizine Hydrochloride (Allergy) is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is CETIRIZINE HYDROCHLORIDE.
Product Information
| NDC | 68788-8204 |
|---|---|
| Product ID | 68788-8204_73122009-531b-4929-bf57-494a6fc65b73 |
| Associated GPIs | 41550020100320 |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Cetirizine Hydrochloride (Allergy) |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Cetirizine Hydrochloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | CETIRIZINE HYDROCHLORIDE |
| Labeler Name | Preferred Pharmaceuticals Inc. |
| Pharmaceutical Class | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA090760 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68788-8204-00 (68788820400)
| NDC Package Code | 68788-8204-0 |
|---|---|
| Billing NDC | 68788820400 |
| Package | 100 TABLET in 1 BOTTLE (68788-8204-0) |
| Marketing Start Date | 2022-04-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |