BENZONATATE
- Product NDC
- 61919-517
- 11-digit product format
- 619190517
- Labeler code
- 61919
- Product ID
- 61919-517_ea4e7175-945e-6be8-e053-2a95a90a507c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENZONATATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA040749
- Marketing category
- ANDA
- Marketing start
- 2019-07-30
- 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
- 2023-12-31
- 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 |
|---|
| 61919-517-30 | BENZONATATE | 30 in 1 BOTTLE | CAPSULE | 30 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-517 | BENZONATATE CAPSULE [DIRECT RX] | 5 | Legacy NDC, 1 package rows | 20190404_2c3483d2-488d-41d9-9bfb-49e7dc64e307.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 |
|---|
| 61919-517-20 | 61919051720 | 20 CAPSULE in 1 BOTTLE (61919-517-20) | 20 capsule | 2019-07-30 | 0000-00-00 | No | No | Current |
| 61919-517-30 | 61919051730 | 30 CAPSULE in 1 BOTTLE (61919-517-30) | 30 capsule | 2019-04-03 | 0000-00-00 | No | No | Current |