benzonatate
- Product NDC
- 63629-1051
- 11-digit product format
- 636291051
- Labeler code
- 63629
- Product ID
- 63629-1051_a75b893d-842f-481d-a66c-fc5b899fea54
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040627
- Marketing category
- ANDA
- Marketing start
- 2017-03-22
- 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
- 2020-12-31
- 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 |
|---|
| 63629-1051-1 | 63629105101 | 1 CAPSULE in 1 BOTTLE (63629-1051-1) | 1 capsule | 2017-03-22 | 0000-00-00 | No | No | Current |