benzonatate
- Product NDC
- 0904-5904
- 11-digit product format
- 009045904
- Labeler code
- 0904
- Product ID
- 0904-5904_f27f6ee9-9142-40e8-bc11-147f7af25e39
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA040627
- Marketing category
- ANDA
- Marketing start
- 2007-07-25
- Marketing end
- 2021-03-31
- 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
- 0000-00-00
- 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 |
|---|
| 0904-5904-60 | 00904590460 | 100 CAPSULE in 1 BOTTLE (0904-5904-60) | 100 capsule | 2007-07-25 | 2021-03-31 | No | No | Current |