benzonatate
- Product NDC
- 50090-4390
- 11-digit product format
- 500904390
- Labeler code
- 50090
- Product ID
- 50090-4390_b46ed419-fc49-43cd-9f6a-4b9795eeed1c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040627
- Marketing category
- ANDA
- Marketing start
- 2017-03-22
- 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
- 2021-12-31
- 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 |
|---|
| 50090-4390-0 | benzonatate | 15 in 1 BOTTLE | CAPSULE | 15 | | 1 |
| 50090-4390-1 | 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 |
|---|
| 50090-4390 | BENZONATATE CAPSULE [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20200711_c69b2d08-0764-433b-85a6-b04c7c2c9498.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 |
|---|
| 50090-4390-0 | 50090439000 | 15 CAPSULE in 1 BOTTLE (50090-4390-0) | 15 capsule | 2019-06-27 | 0000-00-00 | No | No | Current |
| 50090-4390-1 | 50090439001 | 15 CAPSULE in 1 BOTTLE (50090-4390-1) | 15 capsule | 2019-06-27 | 0000-00-00 | No | No | Current |