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Diabecline
Diabecline - 24471-200-20 - (Tetracycline hydrochloride)
Drug Information of Diabecline
| Product NDC: | 24471-200 |
| Proprietary Name: | Diabecline |
| Non Proprietary Name: | Tetracycline hydrochloride |
| Active Ingredient(s): | 30 mg/mL & nbsp; Tetracycline hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diabecline
| Product NDC: | 24471-200 |
| Labeler Name: | THRU PHARMA, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130523 |
Package Information of Diabecline
| Package NDC: | 24471-200-20 |
| Package Description: | 10 TUBE, WITH APPLICATOR in 1 BOX (24471-200-20) > 1.1 mL in 1 TUBE, WITH APPLICATOR |
NDC Information of Diabecline
| NDC Code | 24471-200-20 |
| Proprietary Name | Diabecline |
| Package Description | 10 TUBE, WITH APPLICATOR in 1 BOX (24471-200-20) > 1.1 mL in 1 TUBE, WITH APPLICATOR |
| Product NDC | 24471-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tetracycline hydrochloride |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20130523 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | THRU PHARMA, LLC |
| Substance Name | TETRACYCLINE HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
