benzonatate
- Product NDC
- 55700-561
- 11-digit product format
- 557000561
- Labeler code
- 55700
- Product ID
- 55700-561_2901aa20-7fe4-4488-ac08-0acc63d8efaf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA040749
- Marketing category
- ANDA
- Marketing start
- 2017-11-17
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-561-20 | 55700056120 | 20 CAPSULE in 1 BOTTLE (55700-561-20) | 20 capsule | 2017-11-17 | 0000-00-00 | No | No | Current |
| 55700-561-30 | 55700056130 | 30 CAPSULE in 1 BOTTLE (55700-561-30) | 30 capsule | 2017-11-17 | 0000-00-00 | No | No | Current |