Benzonatate
- Product NDC
- 68788-6839
- 11-digit product format
- 687886839
- Labeler code
- 68788
- Product ID
- 68788-6839_2f3cbe8f-4a6f-4a18-9235-d5cc731c2244
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202765
- Marketing category
- ANDA
- Marketing start
- 2016-12-05
- Marketing end
- 0000-00-00
- Substance
- BENZONATATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record