Product NDC: | 43074-108 |
Proprietary Name: | Dyabetex |
Non Proprietary Name: | TETRACYCLINE HYDROCHLORIDE |
Active Ingredient(s): | .03 mg/mL & nbsp; TETRACYCLINE HYDROCHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43074-108 |
Labeler Name: | Phillips Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100824 |
Package NDC: | 43074-108-02 |
Package Description: | 1 BOTTLE, DROPPER in 1 BOTTLE, PLASTIC (43074-108-02) > 3 mL in 1 BOTTLE, DROPPER (43074-108-01) |
NDC Code | 43074-108-02 |
Proprietary Name | Dyabetex |
Package Description | 1 BOTTLE, DROPPER in 1 BOTTLE, PLASTIC (43074-108-02) > 3 mL in 1 BOTTLE, DROPPER (43074-108-01) |
Product NDC | 43074-108 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TETRACYCLINE HYDROCHLORIDE |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20100824 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Phillips Company |
Substance Name | TETRACYCLINE HYDROCHLORIDE |
Strength Number | .03 |
Strength Unit | mg/mL |
Pharmaceutical Classes |