NDC 68382-091 – Benzonatate
Benzonatate 200 mg/1 · Capsule, Liquid Filled · Oral
Product NDC68382-091
Product details
- Brand name
- Benzonatate
- Generic name
- Benzonatate
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Capsule, Liquid Filled
- Route
- Oral
- Marketing category
- ANDA · ANDA040597
- Marketed since
- April 9, 2007
- Listing expires
- December 31, 2027
- Pharmacologic class
- Non-narcotic Antitussive
Active ingredients
- Benzonatate 200 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68382-091-01 | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (68382-091-01) | Apr 9, 2007 |
Recalls mentioning this NDC
- D-0325-2015 Dec 31, 2014 · Class II
Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.
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