Benzonatate 65841-0843
Product NDC
65841-0843- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 4, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA040597
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Benzonatate | 200 mg/1 |
Drug Class
Non-narcotic Antitussive [EPC]Decreased Tracheobronchial Stretch Receptor Activity [PE]Non-narcotic Antitussive [EPC]
Packaging Options(1)
100 CAPSULE in 1 BOTTLE (65841-843-01)