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ENJUVIA
ENJUVIA - 54868-6165-1 - (synthetic conjugated estrogens, B)
Drug Information of ENJUVIA
| Product NDC: | 54868-6165 |
| Proprietary Name: | ENJUVIA |
| Non Proprietary Name: | synthetic conjugated estrogens, B |
| Active Ingredient(s): | .9 mg/1 & nbsp; synthetic conjugated estrogens, B |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ENJUVIA
| Product NDC: | 54868-6165 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021443 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100903 |
Package Information of ENJUVIA
| Package NDC: | 54868-6165-1 |
| Package Description: | 30 TABLET in 1 BOTTLE (54868-6165-1) |
NDC Information of ENJUVIA
| NDC Code | 54868-6165-1 |
| Proprietary Name | ENJUVIA |
| Package Description | 30 TABLET in 1 BOTTLE (54868-6165-1) |
| Product NDC | 54868-6165 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | synthetic conjugated estrogens, B |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100903 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ESTROGENS, CONJUGATED SYNTHETIC B |
| Strength Number | .9 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
