Benzonatate
- Product NDC
- 66267-765
- 11-digit product format
- 662670765
- Labeler code
- 66267
- Product ID
- 66267-765_9cadc4db-41ad-004a-e053-2a95a90a2528
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA040597
- Marketing category
- ANDA
- Marketing start
- 2007-04-09
- 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
- 2021-12-31
- 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 |
|---|
| 66267-765-06 | 66267076506 | 6 CAPSULE in 1 BOTTLE (66267-765-06) | 6 capsule | 2017-01-03 | 0000-00-00 | No | No | Current |