benzonatate
- Product NDC
- 68071-4258
- 11-digit product format
- 680714258
- Labeler code
- 68071
- Product ID
- 68071-4258_bb789b4d-e783-b42d-e053-2a95a90ac965
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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 |
|---|
| 68071-4258-2 | 68071425802 | 20 CAPSULE in 1 BOTTLE (68071-4258-2) | 20 capsule | 2018-01-29 | 0000-00-00 | No | No | Current |
| 68071-4258-3 | 68071425803 | 30 CAPSULE in 1 BOTTLE (68071-4258-3) | 30 capsule | 2018-01-29 | 0000-00-00 | No | No | Current |
| 68071-4258-6 | 68071425806 | 60 CAPSULE in 1 BOTTLE (68071-4258-6) | 60 capsule | 2018-01-29 | 0000-00-00 | No | No | Current |