benzonatate
- Product NDC
- 50090-3246
- 11-digit product format
- 500903246
- Labeler code
- 50090
- Product ID
- 50090-3246_66ba6922-869f-4e97-a95a-6cac59065924
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040749
- Marketing category
- ANDA
- Marketing start
- 2017-03-22
- 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
- 2022-12-31
- 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 |
|---|
| 50090-3246-0 | 50090324600 | 30 CAPSULE in 1 BOTTLE (50090-3246-0) | 30 capsule | 2017-11-06 | 0000-00-00 | No | No | Current |
| 50090-3246-1 | 50090324601 | 45 CAPSULE in 1 BOTTLE (50090-3246-1) | 45 capsule | 2017-11-06 | 0000-00-00 | No | No | Current |
| 50090-3246-2 | 50090324602 | 15 CAPSULE in 1 BOTTLE (50090-3246-2) | 15 capsule | 2018-04-16 | 0000-00-00 | No | No | Current |