Home
>
National Drug Code (NDC)
>
Zonatuss
Zonatuss - 59702-150-01 - (benzonatate)
Drug Information of Zonatuss
| Product NDC: | 59702-150 |
| Proprietary Name: | Zonatuss |
| Non Proprietary Name: | benzonatate |
| Active Ingredient(s): | 150 mg/1 & nbsp; benzonatate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zonatuss
| Product NDC: | 59702-150 |
| Labeler Name: | Atley Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040851 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100226 |
Package Information of Zonatuss
| Package NDC: | 59702-150-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (59702-150-01) |
NDC Information of Zonatuss
| NDC Code | 59702-150-01 |
| Proprietary Name | Zonatuss |
| Package Description | 100 CAPSULE in 1 BOTTLE (59702-150-01) |
| Product NDC | 59702-150 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benzonatate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100226 |
| Marketing Category Name | ANDA |
| Labeler Name | Atley Pharmaceuticals |
| Substance Name | BENZONATATE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC] |
