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MEGESTOL
MEGESTOL - 16590-898-08 - (MEGESTROL ACETATE)
Drug Information of MEGESTOL
| Product NDC: | 16590-898 |
| Proprietary Name: | MEGESTOL |
| Non Proprietary Name: | MEGESTROL ACETATE |
| Active Ingredient(s): | 40 mg/mL & nbsp; MEGESTROL ACETATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MEGESTOL
| Product NDC: | 16590-898 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075997 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020215 |
Package Information of MEGESTOL
| Package NDC: | 16590-898-08 |
| Package Description: | 240 mL in 1 BOTTLE, PLASTIC (16590-898-08) |
NDC Information of MEGESTOL
| NDC Code | 16590-898-08 |
| Proprietary Name | MEGESTOL |
| Package Description | 240 mL in 1 BOTTLE, PLASTIC (16590-898-08) |
| Product NDC | 16590-898 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MEGESTROL ACETATE |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20020215 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | MEGESTROL ACETATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
