Benzonatate
- Product NDC
- 67296-1371
- 11-digit product format
- 672961371
- Labeler code
- 67296
- Product ID
- 67296-1371_9c9f954d-580b-3cfa-e053-2a95a90a6cda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA081297
- Marketing category
- ANDA
- Marketing start
- 2015-06-01
- 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 |
|---|
| 67296-1371-7 | Benzonatate | 15 in 1 BOTTLE | CAPSULE | 15 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1371 | BENZONATATE CAPSULE [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 1 package rows | 20200121_50497c81-882a-0707-e054-00144ff88e88.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 |
|---|
| 67296-1371-7 | 67296137107 | 15 CAPSULE in 1 BOTTLE (67296-1371-7) | 15 capsule | 2015-06-01 | 0000-00-00 | No | No | Current |