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Cervidil
Cervidil - 0456-4123-63 - (Dinoprostone)
Drug Information of Cervidil
| Product NDC: | 0456-4123 |
| Proprietary Name: | Cervidil |
| Non Proprietary Name: | Dinoprostone |
| Active Ingredient(s): | 10 mg/1 & nbsp; Dinoprostone |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | INSERT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cervidil
| Product NDC: | 0456-4123 |
| Labeler Name: | Forest Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020411 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19950519 |
Package Information of Cervidil
| Package NDC: | 0456-4123-63 |
| Package Description: | 1 INSERT in 1 PACKET (0456-4123-63) |
NDC Information of Cervidil
| NDC Code | 0456-4123-63 |
| Proprietary Name | Cervidil |
| Package Description | 1 INSERT in 1 PACKET (0456-4123-63) |
| Product NDC | 0456-4123 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dinoprostone |
| Dosage Form Name | INSERT |
| Route Name | VAGINAL |
| Start Marketing Date | 19950519 |
| Marketing Category Name | NDA |
| Labeler Name | Forest Laboratories, Inc. |
| Substance Name | DINOPROSTONE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient] |
