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HUMATROPE
HUMATROPE - 0002-7335-11 - (Somatropin)
Drug Information of HUMATROPE
| Product NDC: | 0002-7335 |
| Proprietary Name: | HUMATROPE |
| Non Proprietary Name: | Somatropin |
| Active Ingredient(s): | & nbsp; Somatropin |
| Administration Route(s): | INTRAMUSCULAR; SUBCUTANEOUS |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HUMATROPE
| Product NDC: | 0002-7335 |
| Labeler Name: | Eli Lilly and Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019640 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19870401 |
Package Information of HUMATROPE
| Package NDC: | 0002-7335-11 |
| Package Description: | 1 KIT in 1 CARTON (0002-7335-11) * 5 mL in 1 VIAL (0002-7349-01) * 5 mL in 1 VIAL (0002-7336-01) |
NDC Information of HUMATROPE
| NDC Code | 0002-7335-11 |
| Proprietary Name | HUMATROPE |
| Package Description | 1 KIT in 1 CARTON (0002-7335-11) * 5 mL in 1 VIAL (0002-7349-01) * 5 mL in 1 VIAL (0002-7336-01) |
| Product NDC | 0002-7335 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Somatropin |
| Dosage Form Name | KIT |
| Route Name | INTRAMUSCULAR; SUBCUTANEOUS |
| Start Marketing Date | 19870401 |
| Marketing Category Name | NDA |
| Labeler Name | Eli Lilly and Company |
| Substance Name | |
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