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Sterile Diluent
Sterile Diluent - 0002-0800-01 - (diluent)
Drug Information of Sterile Diluent
| Product NDC: | 0002-0800 |
| Proprietary Name: | Sterile Diluent |
| Non Proprietary Name: | diluent |
| Active Ingredient(s): | 1 mL/mL & nbsp; diluent |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sterile Diluent
| Product NDC: | 0002-0800 |
| Labeler Name: | Eli Lilly and Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA018781 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19990201 |
Package Information of Sterile Diluent
| Package NDC: | 0002-0800-01 |
| Package Description: | 1 VIAL in 1 CARTON (0002-0800-01) > 10 mL in 1 VIAL |
NDC Information of Sterile Diluent
| NDC Code | 0002-0800-01 |
| Proprietary Name | Sterile Diluent |
| Package Description | 1 VIAL in 1 CARTON (0002-0800-01) > 10 mL in 1 VIAL |
| Product NDC | 0002-0800 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | diluent |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 19990201 |
| Marketing Category Name | NDA |
| Labeler Name | Eli Lilly and Company |
| Substance Name | WATER |
| Strength Number | 1 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
