benzonatate
- Product NDC
- 63739-029
- 11-digit product format
- 637390029
- Labeler code
- 63739
- Product ID
- 63739-029_b48e9970-e4a5-2779-e053-2a95a90a1bb0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benzonatate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- 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
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-029-10 | 63739002910 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-029-10) > 10 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2017-03-29 | 0000-00-00 | No | No | Current |