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GENOTROPIN
GENOTROPIN - 0013-2652-02 - (somatropin)
Drug Information of GENOTROPIN
| Product NDC: | 0013-2652 |
| Proprietary Name: | GENOTROPIN |
| 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 GENOTROPIN
| Product NDC: | 0013-2652 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020280 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19951220 |
Package Information of GENOTROPIN
| Package NDC: | 0013-2652-02 |
| Package Description: | 7 CARTRIDGE in 1 CARTON (0013-2652-02) > 1 KIT in 1 CARTRIDGE |
NDC Information of GENOTROPIN
| NDC Code | 0013-2652-02 |
| Proprietary Name | GENOTROPIN |
| Package Description | 7 CARTRIDGE in 1 CARTON (0013-2652-02) > 1 KIT in 1 CARTRIDGE |
| Product NDC | 0013-2652 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | somatropin |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19951220 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
