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NDC 70518-1265-01 Hydroxyzine hydrochloride 50 mg/1 Details
Hydroxyzine hydrochloride 50 mg/1
Hydroxyzine hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is HYDROXYZINE DIHYDROCHLORIDE.
Product Information
| NDC | 70518-1265 |
|---|---|
| Product ID | 70518-1265_02a9cdf7-6f43-55dd-e063-6294a90a25d2 |
| Associated GPIs | |
| 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 | Hydroxyzine hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Hydroxyzine hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/1 |
| Substance Name | HYDROXYZINE DIHYDROCHLORIDE |
| Labeler Name | REMEDYREPACK INC. |
| Pharmaceutical Class | Antihistamine [EPC], Histamine Receptor Antagonists [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA204279 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70518-1265-01 (70518126501)
| NDC Package Code | 70518-1265-1 |
|---|---|
| Billing NDC | 70518126501 |
| Package | 60 TABLET in 1 BOTTLE, PLASTIC (70518-1265-1) |
| Marketing Start Date | 2022-10-25 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |