BENZONATATE
- Product NDC
- 61919-763
- 11-digit product format
- 619190763
- Labeler code
- 61919
- Product ID
- 61919-763_2bd5ca08-ac44-2b22-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENZONATATE
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA202765
- Marketing category
- ANDA
- Marketing start
- 2016-02-15
- 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 |
|---|
| 61919-763-20 | BENZONATATE | 20 in 1 BOTTLE | CAPSULE, GELATIN COATED | 20 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-763 | BENZONATATE CAPSULE, GELATIN COATED [DIRECT RX] | 1 | Legacy NDC, 1 package rows | 20160216_2bd5ca08-ac43-2b22-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-763-20 | 61919076320 | 20 in 1 BOTTLE | Historical |