Benzonatate
- Product NDC
- 68788-7560
- 11-digit product format
- 687887560
- Labeler code
- 68788
- Product ID
- 68788-7560_c3b6e571-87b3-4de5-9d88-76e6c2d53a8a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA206948
- Marketing category
- ANDA
- Marketing start
- 2018-12-21
- 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
- 2023-12-31
- 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 |
|---|
| 68788-7560-1 | 68788756001 | 15 CAPSULE in 1 BOTTLE (68788-7560-1) | 15 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7560-2 | 68788756002 | 20 CAPSULE in 1 BOTTLE (68788-7560-2) | 20 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7560-3 | 68788756003 | 30 CAPSULE in 1 BOTTLE (68788-7560-3) | 30 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7560-6 | 68788756006 | 60 CAPSULE in 1 BOTTLE (68788-7560-6) | 60 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |