BENZONATATE
- Product NDC
- 55700-922
- 11-digit product format
- 557000922
- Labeler code
- 55700
- Product ID
- 55700-922_87589df0-c858-44fe-9b5e-770865751a01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENZONATATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA040682
- Marketing category
- ANDA
- Marketing start
- 2021-08-17
- 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 |
|---|
| 55700-922-30 | 55700092230 | 30 CAPSULE in 1 BOTTLE (55700-922-30) | 30 capsule | 2021-08-17 | 0000-00-00 | No | No | Current |