Benzonatate
- Product NDC
- 70934-058
- 11-digit product format
- 709340058
- Labeler code
- 70934
- Product ID
- 70934-058_d22b4c9b-ba18-2eb7-e053-2a95a90a7c6a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA040597
- Marketing category
- ANDA
- Marketing start
- 2019-10-14
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-058-30 | 70934005830 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-058-30) | 30 capsule | 2018-01-02 | 0000-00-00 | No | No | Current |