Home
>
National Drug Code (NDC)
>
Cleanize
Cleanize - 44929-001-02 - (sodium chloride)
Drug Information of Cleanize
| Product NDC: | 44929-001 |
| Proprietary Name: | Cleanize |
| Non Proprietary Name: | sodium chloride |
| Active Ingredient(s): | 900 mg/100mL & nbsp; sodium chloride |
| Administration Route(s): | NASAL; OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cleanize
| Product NDC: | 44929-001 |
| Labeler Name: | Laboratoires Gifrer Barbezat |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20081125 |
Package Information of Cleanize
| Package NDC: | 44929-001-02 |
| Package Description: | 20 AMPULE in 1 CARTON (44929-001-02) > 5 mL in 1 AMPULE (44929-001-01) |
NDC Information of Cleanize
| NDC Code | 44929-001-02 |
| Proprietary Name | Cleanize |
| Package Description | 20 AMPULE in 1 CARTON (44929-001-02) > 5 mL in 1 AMPULE (44929-001-01) |
| Product NDC | 44929-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sodium chloride |
| Dosage Form Name | SOLUTION |
| Route Name | NASAL; OPHTHALMIC |
| Start Marketing Date | 20081125 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Laboratoires Gifrer Barbezat |
| Substance Name | SODIUM CHLORIDE |
| Strength Number | 900 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
