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Misoprostol
Misoprostol - 40032-161-06 - (Misoprostol)
Drug Information of Misoprostol
| Product NDC: | 40032-161 |
| 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) |
Labeler Information of Misoprostol
| Product NDC: | 40032-161 |
| Labeler Name: | Novel Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091667 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120725 |
Package Information of Misoprostol
| Package NDC: | 40032-161-06 |
| Package Description: | 60 TABLET in 1 BOTTLE (40032-161-06) |
NDC Information of Misoprostol
| NDC Code | 40032-161-06 |
| Proprietary Name | Misoprostol |
| Package Description | 60 TABLET in 1 BOTTLE (40032-161-06) |
| Product NDC | 40032-161 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Misoprostol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120725 |
| Marketing Category Name | ANDA |
| Labeler Name | Novel Laboratories, Inc. |
| Substance Name | MISOPROSTOL |
| Strength Number | 200 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [Chemical/Ingredient] |
