Benzonatate
- Product NDC
- 68788-7569
- 11-digit product format
- 687887569
- Labeler code
- 68788
- Product ID
- 68788-7569_058bd5ae-27c7-4e03-8292-10a32840e94b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA081297
- Marketing category
- ANDA
- Marketing start
- 2016-08-15
- Marketing end
- 0000-00-00
- Substance
- BENZONATATE
- Active strength
- 100 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7569-0 | 68788756900 | 9 CAPSULE in 1 BOTTLE, PLASTIC (68788-7569-0) | 9 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7569-1 | 68788756901 | 100 CAPSULE in 1 BOTTLE, GLASS (68788-7569-1) | 100 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7569-2 | 68788756902 | 20 CAPSULE in 1 BOTTLE, PLASTIC (68788-7569-2) | 20 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7569-3 | 68788756903 | 30 CAPSULE in 1 BOTTLE, PLASTIC (68788-7569-3) | 30 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7569-4 | 68788756904 | 40 CAPSULE in 1 BOTTLE, PLASTIC (68788-7569-4) | 40 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7569-5 | 68788756905 | 15 CAPSULE in 1 BOTTLE, PLASTIC (68788-7569-5) | 15 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7569-9 | 68788756909 | 90 CAPSULE in 1 BOTTLE, PLASTIC (68788-7569-9) | 90 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |