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Armarita
Armarita - 53028-1001-2 - (Sulfur)
Drug Information of Armarita
| Product NDC: | 53028-1001 |
| Proprietary Name: | Armarita |
| Non Proprietary Name: | Sulfur |
| Active Ingredient(s): | .12 mg/3mL & nbsp; Sulfur |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Armarita
| Product NDC: | 53028-1001 |
| Labeler Name: | JG Select Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120802 |
Package Information of Armarita
| Package NDC: | 53028-1001-2 |
| Package Description: | 5 SYRINGE, PLASTIC in 1 CARTON (53028-1001-2) > 3 mL in 1 SYRINGE, PLASTIC (53028-1001-1) |
NDC Information of Armarita
| NDC Code | 53028-1001-2 |
| Proprietary Name | Armarita |
| Package Description | 5 SYRINGE, PLASTIC in 1 CARTON (53028-1001-2) > 3 mL in 1 SYRINGE, PLASTIC (53028-1001-1) |
| Product NDC | 53028-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sulfur |
| Dosage Form Name | LIQUID |
| Route Name | VAGINAL |
| Start Marketing Date | 20120802 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | JG Select Inc |
| Substance Name | SULFUR |
| Strength Number | .12 |
| Strength Unit | mg/3mL |
| Pharmaceutical Classes |
