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Omnitrope
Omnitrope - 0781-4004-36 - (Somatropin)
Drug Information of Omnitrope
| Product NDC: | 0781-4004 |
| Proprietary Name: | Omnitrope |
| Non Proprietary Name: | Somatropin |
| Active Ingredient(s): | & nbsp; Somatropin |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Omnitrope
| Product NDC: | 0781-4004 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021426 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060530 |
Package Information of Omnitrope
| Package NDC: | 0781-4004-36 |
| Package Description: | 1 KIT in 1 CARTON (0781-4004-36) * 1 mL in 1 VIAL * 1.14 mL in 1 VIAL |
NDC Information of Omnitrope
| NDC Code | 0781-4004-36 |
| Proprietary Name | Omnitrope |
| Package Description | 1 KIT in 1 CARTON (0781-4004-36) * 1 mL in 1 VIAL * 1.14 mL in 1 VIAL |
| Product NDC | 0781-4004 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Somatropin |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20060530 |
| Marketing Category Name | NDA |
| Labeler Name | Sandoz Inc |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
