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Humulin
Humulin - 0002-8315-17 - (Insulin human)
Drug Information of Humulin
| Product NDC: | 0002-8315 |
| Proprietary Name: | Humulin |
| Non Proprietary Name: | Insulin human |
| Active Ingredient(s): | 100 [iU]/mL & nbsp; Insulin human |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Humulin
| Product NDC: | 0002-8315 |
| Labeler Name: | Eli Lilly and Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA018781 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19830627 |
Package Information of Humulin
| Package NDC: | 0002-8315-17 |
| Package Description: | 1 VIAL in 1 CARTON (0002-8315-17) > 3 mL in 1 VIAL |
NDC Information of Humulin
| NDC Code | 0002-8315-17 |
| Proprietary Name | Humulin |
| Package Description | 1 VIAL in 1 CARTON (0002-8315-17) > 3 mL in 1 VIAL |
| Product NDC | 0002-8315 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Insulin human |
| Dosage Form Name | INJECTION, SUSPENSION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 19830627 |
| Marketing Category Name | NDA |
| Labeler Name | Eli Lilly and Company |
| Substance Name | INSULIN HUMAN |
| Strength Number | 100 |
| Strength Unit | [iU]/mL |
| Pharmaceutical Classes |
