Product NDC: | 59762-5008 |
Proprietary Name: | misoprostol |
Non Proprietary Name: | MISOPROSTOL |
Active Ingredient(s): | 200 ug/1 & nbsp; MISOPROSTOL |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59762-5008 |
Labeler Name: | Greenstone LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019268 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20091227 |
Package NDC: | 59762-5008-2 |
Package Description: | 100 TABLET in 1 BOTTLE (59762-5008-2) |
NDC Code | 59762-5008-2 |
Proprietary Name | misoprostol |
Package Description | 100 TABLET in 1 BOTTLE (59762-5008-2) |
Product NDC | 59762-5008 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | MISOPROSTOL |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20091227 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Greenstone LLC |
Substance Name | MISOPROSTOL |
Strength Number | 200 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [Chemical/Ingredient] |