Benzonatate
- Product NDC
- 67296-0567
- 11-digit product format
- 672960567
- Labeler code
- 67296
- Product ID
- 67296-0567_8b3f6f42-e692-4b93-9e10-1537261b6d08
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- RedPharm Drug Inc.
- Application
- ANDA040682
- Marketing category
- ANDA
- Marketing start
- 2010-01-13
- 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
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 67296-0567-1 | Benzonatate | 15 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 15 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0567 | BENZONATATE CAPSULE, LIQUID FILLED [REDPHARM DRUG INC.] | 5 | Legacy NDC, 1 package rows | 20110808_758cced1-db76-41f4-9bdc-d016637a49cf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67296-0567-1 | 67296056701 | 15 in 1 BOTTLE | Historical |