Benzonatate
- Product NDC
- 63629-6690
- 11-digit product format
- 636296690
- Labeler code
- 63629
- Product ID
- 63629-6690_8ba9e35a-35e3-4fba-a172-8addf406b877
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzonatate
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040682
- Marketing category
- ANDA
- Marketing start
- 2010-06-04
- 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
- 2021-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6690-1 | 63629669001 | 21 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-6690-1) | 2015-09-02 | 0000-00-00 | No | No | Current |
| 63629-6690-2 | 63629669002 | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-6690-2) | 2015-09-02 | 0000-00-00 | No | No | Current |