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Nutropin
Nutropin - 50242-018-21 - (Somatropin)
Drug Information of Nutropin
| Product NDC: | 50242-018 |
| Proprietary Name: | Nutropin |
| 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 Nutropin
| Product NDC: | 50242-018 |
| Labeler Name: | Genentech, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019676 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19931117 |
Package Information of Nutropin
| Package NDC: | 50242-018-21 |
| Package Description: | 1 KIT in 1 CARTON (50242-018-21) * 10 mg in 1 VIAL * 10 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Nutropin
| NDC Code | 50242-018-21 |
| Proprietary Name | Nutropin |
| Package Description | 1 KIT in 1 CARTON (50242-018-21) * 10 mg in 1 VIAL * 10 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 50242-018 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Somatropin |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19931117 |
| Marketing Category Name | NDA |
| Labeler Name | Genentech, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
