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Cytotec
Cytotec - 54868-2176-3 - (misoprostol)
Drug Information of Cytotec
| Product NDC: | 54868-2176 |
| Proprietary Name: | Cytotec |
| Non Proprietary Name: | misoprostol |
| Active Ingredient(s): | 100 ug/1 & nbsp; misoprostol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cytotec
| Product NDC: | 54868-2176 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019268 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960702 |
Package Information of Cytotec
| Package NDC: | 54868-2176-3 |
| Package Description: | 40 TABLET in 1 BOTTLE (54868-2176-3) |
NDC Information of Cytotec
| NDC Code | 54868-2176-3 |
| Proprietary Name | Cytotec |
| Package Description | 40 TABLET in 1 BOTTLE (54868-2176-3) |
| Product NDC | 54868-2176 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | misoprostol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19960702 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | MISOPROSTOL |
| Strength Number | 100 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [Chemical/Ingredient] |
