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NDC 51672-4043-03 Clorazepate Dipotassium 7.5 mg/1 Details
Clorazepate Dipotassium 7.5 mg/1
Clorazepate Dipotassium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Taro Pharmaceuticals U.S.A., Inc.. The primary component is CLORAZEPATE DIPOTASSIUM.
MedlinePlus Drug Summary
Clorazepate is used to relieve anxiety. Clorazepate is also used along with other medications to treat certain types of seizures. It is also used to relieve unpleasant symptoms that may be experienced by people who have stopped drinking alcohol after drinking large amounts for a long time. Clorazepate is in a class of medications called benzodiazepines. It works by decreasing abnormal electrical activity in the brain.
Related Packages: 51672-4043-03Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Clorazepate
Product Information
| NDC | 51672-4043 |
|---|---|
| Product ID | 51672-4043_a22613cd-20d8-4b29-8520-d66368b47ea0 |
| Associated GPIs | 57100030100310 |
| GCN Sequence Number | 003746 |
| GCN Sequence Number Description | clorazepate dipotassium TABLET 7.5 MG ORAL |
| HIC3 | H20 |
| HIC3 Description | ANTI-ANXIETY - BENZODIAZEPINES |
| GCN | 14093 |
| HICL Sequence Number | 001612 |
| HICL Sequence Number Description | CLORAZEPATE DIPOTASSIUM |
| Brand/Generic | Generic |
| Proprietary Name | Clorazepate Dipotassium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Clorazepate Dipotassium |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 7.5 |
| Active Ingredient Units | mg/1 |
| Substance Name | CLORAZEPATE DIPOTASSIUM |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Pharmaceutical Class | Benzodiazepine [EPC], Benzodiazepines [CS] |
| DEA Schedule | CIV |
| Marketing Category | ANDA |
| Application Number | ANDA075731 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 51672-4043-03 (51672404303)
| NDC Package Code | 51672-4043-3 |
|---|---|
| Billing NDC | 51672404303 |
| Package | 1000 TABLET in 1 BOTTLE (51672-4043-3) |
| Marketing Start Date | 2000-04-27 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |