Benzonatate
- Product NDC
- 68151-2697
- 11-digit product format
- 681512697
- Labeler code
- 68151
- Product ID
- 68151-2697_016ba14b-397a-48c4-9fc1-e410242fdde6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA040682
- Marketing category
- ANDA
- Marketing start
- 2010-06-04
- 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 |
|---|
| 68151-2697-8 | Benzonatate | 1 in 1 CUP | CAPSULE, LIQUID FILLED | 1 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2697 | BENZONATATE CAPSULE, LIQUID FILLED [CARILION MATERIALS MANAGEMENT] | 11 | Legacy NDC, 1 package rows | 20151224_7ca63723-645c-4516-adaa-8969d3851efe.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2697-8 | 68151269708 | 1 in 1 CUP | Historical |