Benzonatate
- Product NDC
- 67296-1833
- 11-digit product format
- 672961833
- Labeler code
- 67296
- Product ID
- 67296-1833_b78273e5-dbbd-4617-9046-0f0aaba8bb18
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Redpharm drug, inc
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Benzonatate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZONATATE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5P4DHS6ENR |
| Rxcui | 283417 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1833-3 | Benzonatate | 30 in 1 BOTTLE | CAPSULE | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1833 | BENZONATATE CAPSULE [REDPHARM DRUG, INC] | 2 | Current NDC, 1 package rows | 20240719_f3c23663-0cb7-ffa4-e053-2a95a90a9ae0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-1833-3 | 67296183303 | 30 CAPSULE in 1 BOTTLE (67296-1833-3) | 30 capsule | 2019-02-22 | No | No | Historical |