BENZONATATE
- Product NDC
- 68788-8127
- 11-digit product format
- 687888127
- Labeler code
- 68788
- Product ID
- 68788-8127_616e7683-0f2a-459c-95ac-eecc0a26ed60
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENZONATATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA040682
- Marketing category
- ANDA
- Marketing start
- 2022-01-17
- 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 |
|---|
| 68788-8127-1 | 68788812701 | 15 CAPSULE in 1 BOTTLE (68788-8127-1) | 15 capsule | 2022-01-17 | 0000-00-00 | No | No | Current |
| 68788-8127-2 | 68788812702 | 20 CAPSULE in 1 BOTTLE (68788-8127-2) | 20 capsule | 2022-01-17 | 0000-00-00 | No | No | Current |
| 68788-8127-3 | 68788812703 | 30 CAPSULE in 1 BOTTLE (68788-8127-3) | 30 capsule | 2022-01-17 | 0000-00-00 | No | No | Current |
| 68788-8127-6 | 68788812706 | 60 CAPSULE in 1 BOTTLE (68788-8127-6) | 60 capsule | 2022-01-17 | 0000-00-00 | No | No | Current |