Benzonatate
- Product NDC
- 65841-615
- 11-digit product format
- 658410615
- Labeler code
- 65841
- Product ID
- 65841-615_dfbdfc10-d5cc-460b-b144-134e1cc87583
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cadila Healthcare Limited
- Application
- ANDA040597
- Marketing category
- ANDA
- Marketing start
- 2007-09-04
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65841-615-01 | 65841061501 | 100 CAPSULE in 1 BOTTLE (65841-615-01) | 100 capsule | 2007-09-04 | 0000-00-00 | No | No | Current |