Benzonatate
- Product NDC
- 55154-7995
- 11-digit product format
- 551547995
- Labeler code
- 55154
- Product ID
- 55154-7995_761ce0b3-1ae1-4a95-8a66-617b76fdb81e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA040597
- Marketing category
- ANDA
- Marketing start
- 2007-09-04
- 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
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-7995-0 | 55154799500 | 10 BLISTER PACK in 1 BAG (55154-7995-0) > 1 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2007-09-04 | 0000-00-00 | No | No | Current |