benzonatate
- Product NDC
- 68788-7087
- 11-digit product format
- 687887087
- Labeler code
- 68788
- Product ID
- 68788-7087_6496a977-cacb-430a-8c7a-e13d44d9c55c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc
- Application
- ANDA040749
- Marketing category
- ANDA
- Marketing start
- 2018-01-26
- 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
- 2022-12-31
- 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 |
|---|
| 68788-7087-1 | 68788708701 | 15 CAPSULE in 1 BOTTLE (68788-7087-1) | 15 capsule | 2018-01-26 | 0000-00-00 | No | No | Current |
| 68788-7087-2 | 68788708702 | 20 CAPSULE in 1 BOTTLE (68788-7087-2) | 20 capsule | 2018-01-26 | 0000-00-00 | No | No | Current |
| 68788-7087-3 | 68788708703 | 30 CAPSULE in 1 BOTTLE (68788-7087-3) | 30 capsule | 2018-01-26 | 0000-00-00 | No | No | Current |
| 68788-7087-6 | 68788708706 | 60 CAPSULE in 1 BOTTLE (68788-7087-6) | 60 capsule | 2018-01-26 | 0000-00-00 | No | No | Current |