Benzonatate 42708-0082
Product NDC
42708-0082- Manufacturer
- Qpharma, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 22, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA040627
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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)
21 CAPSULE in 1 BOTTLE (42708-082-21)