Benzonatate
- Product NDC
- 65841-843
- 11-digit product format
- 658410843
- Labeler code
- 65841
- Product ID
- 65841-843_fb123061-e971-4394-aa10-ae733de31be1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA040597
- Marketing category
- ANDA
- Marketing start
- 2007-09-04
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Benzonatate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZONATATE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5P4DHS6ENR |
| Rxcui | 197397, 283417 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 65841-843-01 | Benzonatate | 100 in 1 BOTTLE | CAPSULE | 100 | | 9 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65841-843 | BENZONATATE CAPSULE [ZYDUS LIFESCIENCES LIMITED] | 9 | Current NDC, Legacy NDC, 1 package rows | 20241128_abb4360a-4c52-45b6-9b80-df3c1bfc4c59.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 |
|---|
| 65841-843-01 | 65841084301 | 100 CAPSULE in 1 BOTTLE (65841-843-01) | 100 capsule | 2007-09-04 | 0000-00-00 | No | No | Current |