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Chlorhexidine Gluconate
Chlorhexidine Gluconate - 21695-025-16 - (Chlorhexidine Gluconate)
Drug Information of Chlorhexidine Gluconate
| Product NDC: | 21695-025 |
| Proprietary Name: | Chlorhexidine Gluconate |
| Non Proprietary Name: | Chlorhexidine Gluconate |
| Active Ingredient(s): | .12 mg/mL & nbsp; Chlorhexidine Gluconate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | RINSE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlorhexidine Gluconate
| Product NDC: | 21695-025 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077789 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090801 |
Package Information of Chlorhexidine Gluconate
| Package NDC: | 21695-025-16 |
| Package Description: | 473 mL in 1 BOTTLE (21695-025-16) |
NDC Information of Chlorhexidine Gluconate
| NDC Code | 21695-025-16 |
| Proprietary Name | Chlorhexidine Gluconate |
| Package Description | 473 mL in 1 BOTTLE (21695-025-16) |
| Product NDC | 21695-025 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlorhexidine Gluconate |
| Dosage Form Name | RINSE |
| Route Name | ORAL |
| Start Marketing Date | 20090801 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CHLORHEXIDINE GLUCONATE |
| Strength Number | .12 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Cell Wall Integrity [PE] |
