Benzonatate
- Product NDC
- 50090-5823
- 11-digit product format
- 500905823
- Labeler code
- 50090
- Product ID
- 50090-5823_8a95c5be-0141-4ae9-a340-fbe4c64ebd7c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202765
- Marketing category
- ANDA
- Marketing start
- 2015-08-10
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-5823-0 | Benzonatate | 30 in 1 BOTTLE | CAPSULE | 30 | | 1 |
| 50090-5823-1 | Benzonatate | 45 in 1 BOTTLE | CAPSULE | 45 | | 1 |
| 50090-5823-2 | Benzonatate | 15 in 1 BOTTLE | CAPSULE | 15 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5823 | BENZONATATE CAPSULE [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 3 package rows | 20211030_dac32ac4-c047-4321-94ef-ee2994835618.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5823-0 | 50090582300 | 30 CAPSULE in 1 BOTTLE (50090-5823-0) | 30 capsule | 2021-10-22 | 0000-00-00 | No | No | Current |
| 50090-5823-1 | 50090582301 | 45 CAPSULE in 1 BOTTLE (50090-5823-1) | 45 capsule | 2021-10-22 | 0000-00-00 | No | No | Current |
| 50090-5823-2 | 50090582302 | 15 CAPSULE in 1 BOTTLE (50090-5823-2) | 15 capsule | 2021-10-22 | 0000-00-00 | No | No | Current |