Benzonatate
- Product NDC
- 68071-4105
- 11-digit product format
- 680714105
- Labeler code
- 68071
- Product ID
- 68071-4105_5a5a337d-745b-2033-e053-2a91aa0a53f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040597
- Marketing category
- ANDA
- Marketing start
- 2007-04-09
- Marketing end
- 0000-00-00
- Substance
- BENZONATATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record