Benzonatate
- Product NDC
- 50090-6228
- 11-digit product format
- 500906228
- Labeler code
- 50090
- Product ID
- 50090-6228_17123a99-df58-4ff4-a377-d75d68900959
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA211518
- Marketing category
- ANDA
- Marketing start
- 2019-02-22
- 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
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6228 | BENZONATATE CAPSULE [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC | 20231101_8a7cf1ee-f5b1-4013-8eb6-53b6ca23af9b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-6228-0 | 50090622800 | 15 CAPSULE in 1 BOTTLE (50090-6228-0) | 15 capsule | 2022-11-15 | 0000-00-00 | No | No | Current |