Home
>
National Drug Code (NDC)
>
Benzonatate
Benzonatate - 0615-7678-39 - (Benzonatate)
Drug Information of Benzonatate
| Product NDC: | 0615-7678 |
| Proprietary Name: | Benzonatate |
| Non Proprietary Name: | Benzonatate |
| Active Ingredient(s): | 100 mg/1 & nbsp; Benzonatate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Benzonatate
| Product NDC: | 0615-7678 |
| Labeler Name: | NCS HealthCare of KY, Inc dba Vangard Labs |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040597 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070904 |
Package Information of Benzonatate
| Package NDC: | 0615-7678-39 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (0615-7678-39) |
NDC Information of Benzonatate
| NDC Code | 0615-7678-39 |
| Proprietary Name | Benzonatate |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (0615-7678-39) |
| Product NDC | 0615-7678 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Benzonatate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20070904 |
| Marketing Category Name | ANDA |
| Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
| Substance Name | BENZONATATE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC] |
