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misoprostol
misoprostol - 59762-5007-1 - (MISOPROSTOL)
Drug Information of misoprostol
| Product NDC: | 59762-5007 |
| Proprietary Name: | misoprostol |
| 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 misoprostol
| Product NDC: | 59762-5007 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019268 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20091227 |
Package Information of misoprostol
| Package NDC: | 59762-5007-1 |
| Package Description: | 60 TABLET in 1 BOTTLE (59762-5007-1) |
NDC Information of misoprostol
| NDC Code | 59762-5007-1 |
| Proprietary Name | misoprostol |
| Package Description | 60 TABLET in 1 BOTTLE (59762-5007-1) |
| Product NDC | 59762-5007 |
| 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 | 100 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [Chemical/Ingredient] |
