Chlorhexidine Gluconate
- Product NDC
- 50227-0101
- 11-digit product format
- 502270101
- Labeler code
- 50227
- Product ID
- 50227-0101_b60e017f-02a9-5dce-e053-2995a90ac392
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Chlorhexidine Gluconate
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- Patterson Dental Supply Inc.
- Application
- ANDA077789
- Marketing category
- ANDA
- Marketing start
- 2017-06-30
- Marketing end
- 2023-07-31
- 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 |
|---|
| 50227-0101-1 | 50227010101 | 473 mL in 1 BOTTLE, PLASTIC (50227-0101-1) | 473 ml | 2017-06-30 | 2023-07-31 | No | No | Current |
| 50227-0101-4 | 50227010104 | 118 mL in 1 BOTTLE, PLASTIC (50227-0101-4) | 118 ml | 2016-01-22 | 2023-02-28 | No | No | Current |