Chlorhexidine Gluconante
- Product NDC
- 64778-0244
- 11-digit product format
- 647780244
- Labeler code
- 64778
- Product ID
- 64778-0244_efbac109-050b-1a44-e053-2995a90a2873
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorhexidine Gluconante
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- AMD Medicom Inc.
- Application
- ANDA077789
- Marketing category
- ANDA
- Marketing start
- 2006-06-02
- Marketing end
- 2023-05-31
- Substance
- CHLORHEXIDINE GLUCONATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Decreased Cell Wall Integrity [PE]
- 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 |
|---|
| 64778-0244-1 | 64778024401 | 473 mL in 1 BOTTLE, PLASTIC (64778-0244-1) | 473 ml | 2006-06-02 | 0000-00-00 | No | No | Current |