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MENEST
MENEST - 61570-073-01 - (esterified estrogens)
Drug Information of MENEST
| Product NDC: | 61570-073 |
| Proprietary Name: | MENEST |
| Non Proprietary Name: | esterified estrogens |
| Active Ingredient(s): | .625 mg/1 & nbsp; esterified estrogens |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MENEST
| Product NDC: | 61570-073 |
| Labeler Name: | Monarch Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA084948 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19770928 |
Package Information of MENEST
| Package NDC: | 61570-073-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (61570-073-01) |
NDC Information of MENEST
| NDC Code | 61570-073-01 |
| Proprietary Name | MENEST |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (61570-073-01) |
| Product NDC | 61570-073 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | esterified estrogens |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19770928 |
| Marketing Category Name | ANDA |
| Labeler Name | Monarch Pharmaceuticals, Inc. |
| Substance Name | ESTROGENS, ESTERIFIED |
| Strength Number | .625 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
