BENZONATATE
- Product NDC
- 55700-923
- 11-digit product format
- 557000923
- Labeler code
- 55700
- Product ID
- 55700-923_7f5ace25-df79-40f4-80ac-16201472c26a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENZONATATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA040682
- Marketing category
- ANDA
- Marketing start
- 2021-08-16
- 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
- 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 |
|---|
| 55700-923-30 | 55700092330 | 30 CAPSULE in 1 BOTTLE (55700-923-30) | 30 capsule | 2021-08-16 | 0000-00-00 | No | No | Current |