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CHLORHEXIDINE GLUCONATE
CHLORHEXIDINE GLUCONATE - 52376-021-02 - (Chlorhexidine Gluconate)
Drug Information of CHLORHEXIDINE GLUCONATE
| Product NDC: | 52376-021 |
| Proprietary Name: | CHLORHEXIDINE GLUCONATE |
| Non Proprietary Name: | Chlorhexidine Gluconate |
| Active Ingredient(s): | 1.28 mg/g & nbsp; Chlorhexidine Gluconate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | RINSE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CHLORHEXIDINE GLUCONATE
| Product NDC: | 52376-021 |
| Labeler Name: | Sunstar Americas, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076434 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060415 |
Package Information of CHLORHEXIDINE GLUCONATE
| Package NDC: | 52376-021-02 |
| Package Description: | 473 g in 1 BOTTLE, PLASTIC (52376-021-02) |
NDC Information of CHLORHEXIDINE GLUCONATE
| NDC Code | 52376-021-02 |
| Proprietary Name | CHLORHEXIDINE GLUCONATE |
| Package Description | 473 g in 1 BOTTLE, PLASTIC (52376-021-02) |
| Product NDC | 52376-021 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlorhexidine Gluconate |
| Dosage Form Name | RINSE |
| Route Name | ORAL |
| Start Marketing Date | 20060415 |
| Marketing Category Name | ANDA |
| Labeler Name | Sunstar Americas, Inc. |
| Substance Name | CHLORHEXIDINE GLUCONATE |
| Strength Number | 1.28 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Decreased Cell Wall Integrity [PE] |
