BENZONATATE
- Product NDC
- 61919-325
- 11-digit product format
- 619190325
- Labeler code
- 61919
- Product ID
- 61919-325_9f09749c-da04-464b-9964-060e7addc383
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENZONATATE
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA040682
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- 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
- 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 |
|---|
| 61919-325-20 | BENZONATATE | 20 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 20 | | 1 |
| 61919-325-30 | BENZONATATE | 30 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-325 | BENZONATATE CAPSULE, LIQUID FILLED [DIRECTRX] | 1 | Legacy NDC, 2 package rows | 20151027_4b08feeb-5422-47c3-9b70-60cd29ff762d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-325-20 | 61919032520 | 20 in 1 BOTTLE | Historical |
| 61919-325-30 | 61919032530 | 30 in 1 BOTTLE | Historical |