benzonatate
- Product NDC
- 43063-910
- 11-digit product format
- 430630910
- Labeler code
- 43063
- Product ID
- 43063-910_d2be4dbd-f15d-09d6-e053-2a95a90a00d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- 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
- 2022-12-31
- 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 |
|---|
| 43063-910-15 | 43063091015 | 15 CAPSULE in 1 BOTTLE, PLASTIC (43063-910-15) | 15 capsule | 2018-12-06 | 0000-00-00 | No | No | Current |