benzonatate
- Product NDC
- 0179-0237
- 11-digit product format
- 001790237
- Labeler code
- 0179
- Product ID
- 0179-0237_7b2157ee-5f04-a489-e053-2a91aa0a44a1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA040627
- Marketing category
- ANDA
- Marketing start
- 2017-12-20
- Marketing end
- 2020-04-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record