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NDC 70518-0015-00 Chlordiazepoxide Hydrochloride 25 mg/1 Details
Chlordiazepoxide Hydrochloride 25 mg/1
Chlordiazepoxide Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is CHLORDIAZEPOXIDE HYDROCHLORIDE.
MedlinePlus Drug Summary
Chlordiazepoxide is used to relieve anxiety and to control agitation caused by alcohol withdrawal. Chlordiazepoxide is in a class of medications called benzodiazepines. It works by decreasing abnormal electrical activity in the brain.
Related Packages: 70518-0015-00Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Chlordiazepoxide
Product Information
| NDC | 70518-0015 |
|---|---|
| Product ID | 70518-0015_0e0cd179-8677-d1a5-e063-6294a90a7ff8 |
| 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 | Chlordiazepoxide Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Chlordiazepoxide Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CAPSULE |
| Route | ORAL |
| Active Ingredient Strength | 25 |
| Active Ingredient Units | mg/1 |
| Substance Name | CHLORDIAZEPOXIDE HYDROCHLORIDE |
| Labeler Name | REMEDYREPACK INC. |
| Pharmaceutical Class | Benzodiazepine [EPC], Benzodiazepines [CS] |
| DEA Schedule | CIV |
| Marketing Category | ANDA |
| Application Number | ANDA084769 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 70518-0015-00 (70518001500)
| NDC Package Code | 70518-0015-0 |
|---|---|
| Billing NDC | 70518001500 |
| Package | 30 CAPSULE in 1 BLISTER PACK (70518-0015-0) |
| Marketing Start Date | 2016-11-23 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |