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Depo-Estradiol
Depo-Estradiol - 0009-0271-01 - (estradiol cypionate)
Drug Information of Depo-Estradiol
| Product NDC: | 0009-0271 |
| Proprietary Name: | Depo-Estradiol |
| Non Proprietary Name: | estradiol cypionate |
| Active Ingredient(s): | 5 mg/mL & nbsp; estradiol cypionate |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Depo-Estradiol
| Product NDC: | 0009-0271 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085470 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19790815 |
Package Information of Depo-Estradiol
| Package NDC: | 0009-0271-01 |
| Package Description: | 1 VIAL in 1 CARTON (0009-0271-01) > 5 mL in 1 VIAL |
NDC Information of Depo-Estradiol
| NDC Code | 0009-0271-01 |
| Proprietary Name | Depo-Estradiol |
| Package Description | 1 VIAL in 1 CARTON (0009-0271-01) > 5 mL in 1 VIAL |
| Product NDC | 0009-0271 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | estradiol cypionate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 19790815 |
| Marketing Category Name | ANDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | ESTRADIOL CYPIONATE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
