Benzonatate
- Product NDC
- 50090-6080
- 11-digit product format
- 500906080
- Labeler code
- 50090
- Product ID
- 50090-6080_806a317d-630a-4fbd-9e06-d562770d0dd4
- 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
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 5P4DHS6ENR | BENZONATATE | 104-31-4 | BENZONATATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6080-0 | 50090608000 | 30 CAPSULE in 1 BOTTLE (50090-6080-0) | 30 capsule | 2022-09-19 | No | No | Historical |
| 50090-6080-1 | 50090608001 | 45 CAPSULE in 1 BOTTLE (50090-6080-1) | 45 capsule | 2022-09-19 | No | No | Historical |
| 50090-6080-2 | 50090608002 | 15 CAPSULE in 1 BOTTLE (50090-6080-2) | 15 capsule | 2022-09-19 | No | No | Historical |