benzonatate
- Product NDC
- 60760-573
- 11-digit product format
- 607600573
- Labeler code
- 60760
- Product ID
- 60760-573_c6a41cd9-206f-6c85-e053-2995a90a3e00
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA040627
- Marketing category
- ANDA
- Marketing start
- 2018-11-07
- 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 |
|---|
| 60760-573-30 | 60760057330 | 30 CAPSULE in 1 BOTTLE, PLASTIC (60760-573-30) | 30 capsule | 2018-11-07 | 0000-00-00 | No | No | Current |