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Menest
Menest - 54868-6211-1 - (Estrogens, esterified)
Drug Information of Menest
| Product NDC: | 54868-6211 |
| Proprietary Name: | Menest |
| Non Proprietary Name: | Estrogens, esterified |
| Active Ingredient(s): | .3 mg/1 & nbsp; Estrogens, esterified |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Menest
| Product NDC: | 54868-6211 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084951 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101209 |
Package Information of Menest
| Package NDC: | 54868-6211-1 |
| Package Description: | 30 TABLET in 1 BOTTLE, PLASTIC (54868-6211-1) |
NDC Information of Menest
| NDC Code | 54868-6211-1 |
| Proprietary Name | Menest |
| Package Description | 30 TABLET in 1 BOTTLE, PLASTIC (54868-6211-1) |
| Product NDC | 54868-6211 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Estrogens, esterified |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101209 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ESTROGENS, ESTERIFIED |
| Strength Number | .3 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
