Benzonatate
- Product NDC
- 61919-272
- 11-digit product format
- 619190272
- Labeler code
- 61919
- Product ID
- 61919-272_6e5b3652-0803-4b82-afca-da76be9edafb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Direct RX
- Application
- ANDA040682
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- Marketing end
- 0000-00-00
- Substance
- BENZONATATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 61919-272-20 | Benzonatate | 20 in 1 BOTTLE | CAPSULE | 20 | | 2 |
| 61919-272-30 | Benzonatate | 30 in 1 BOTTLE | CAPSULE | 30 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-272 | BENZONATATE CAPSULE [DIRECT RX] | 2 | Legacy NDC, 2 package rows | 20151106_c531b7e1-b248-4b05-9ba8-0fe7a70848a3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-272-20 | 61919027220 | 20 in 1 BOTTLE | Historical |
| 61919-272-30 | 61919027230 | 30 in 1 BOTTLE | Historical |