Chlorhexidine gluconate
- Product NDC
- 48433-214
- 11-digit product format
- 484330214
- Labeler code
- 48433
- Product ID
- 48433-214_3cd1ad6d-814f-4586-9c0e-4cd3ca322bc2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorhexidine gluconate
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- Safecor Health, LLC
- Application
- ANDA077789
- Marketing category
- ANDA
- Marketing start
- 2018-09-14
- Marketing end
- 0000-00-00
- Substance
- CHLORHEXIDINE GLUCONATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Decreased Cell Wall Integrity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48433-214-40 | 48433021440 | 40 CUP, UNIT-DOSE in 1 BOX (48433-214-40) > 15 mL in 1 CUP, UNIT-DOSE (48433-214-15) | 2018-09-14 | 0000-00-00 | No | No | Current |