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Chlorhexidine Gluconate
Chlorhexidine Gluconate - 50383-720-17 - (Chlorhexidine Gluconate)
Drug Information of Chlorhexidine Gluconate
| Product NDC: | 50383-720 |
| Proprietary Name: | Chlorhexidine Gluconate |
| Non Proprietary Name: | Chlorhexidine Gluconate |
| Active Ingredient(s): | 1.2 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: | 50383-720 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074356 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960507 |
Package Information of Chlorhexidine Gluconate
| Package NDC: | 50383-720-17 |
| Package Description: | 4 TRAY in 1 CASE (50383-720-17) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-720-15) > 15 mL in 1 CUP, UNIT-DOSE |
NDC Information of Chlorhexidine Gluconate
| NDC Code | 50383-720-17 |
| Proprietary Name | Chlorhexidine Gluconate |
| Package Description | 4 TRAY in 1 CASE (50383-720-17) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-720-15) > 15 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 50383-720 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlorhexidine Gluconate |
| Dosage Form Name | RINSE |
| Route Name | ORAL |
| Start Marketing Date | 19960507 |
| Marketing Category Name | ANDA |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | CHLORHEXIDINE GLUCONATE |
| Strength Number | 1.2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Cell Wall Integrity [PE] |
