Benzonatate
- Product NDC
- 63629-2444
- 11-digit product format
- 636292444
- Labeler code
- 63629
- Product ID
- 63629-2444_63ed9621-2b87-4528-a9b8-9eb02ea103a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA081297
- Marketing category
- ANDA
- Marketing start
- 2016-08-15
- 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 |
|---|
| 63629-2444-1 | 63629244401 | 100 CAPSULE in 1 BOTTLE, PLASTIC (63629-2444-1) | 100 capsule | 2021-02-16 | 0000-00-00 | No | No | Current |