benzonatate
- Product NDC
- 60687-346
- 11-digit product format
- 606870346
- Labeler code
- 60687
- Product ID
- 60687-346_c32e2997-0c8f-327f-e053-2995a90a8c94
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA040627
- Marketing category
- ANDA
- Marketing start
- 2017-12-07
- Marketing end
- 2022-06-30
- 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 |
|---|
| 60687-346-01 | 60687034601 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-346-01) > 1 CAPSULE in 1 BLISTER PACK (60687-346-11) | 100 blister pack | 2017-12-07 | 0000-00-00 | No | No | Current |