Benzonatate
- Product NDC
- 68788-8133
- 11-digit product format
- 687888133
- Labeler code
- 68788
- Product ID
- 68788-8133_931a262f-a380-4c81-b262-5542c0b2ccf9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc..
- Application
- ANDA081297
- Marketing category
- ANDA
- Marketing start
- 2022-02-03
- 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 |
|---|
| 68788-8133-1 | 68788813301 | 15 CAPSULE in 1 BOTTLE, PLASTIC (68788-8133-1) | 15 capsule | 2022-02-03 | 0000-00-00 | No | No | Current |
| 68788-8133-2 | 68788813302 | 20 CAPSULE in 1 BOTTLE, PLASTIC (68788-8133-2) | 20 capsule | 2022-02-03 | 0000-00-00 | No | No | Current |
| 68788-8133-3 | 68788813303 | 30 CAPSULE in 1 BOTTLE, PLASTIC (68788-8133-3) | 30 capsule | 2022-02-03 | 0000-00-00 | No | No | Current |
| 68788-8133-6 | 68788813306 | 60 CAPSULE in 1 BOTTLE, PLASTIC (68788-8133-6) | 60 capsule | 2022-02-03 | 0000-00-00 | No | No | Current |