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Introvale
Introvale - 0781-5584-36 - (Levonorgestrel and Ethinyl Estradiol)
Drug Information of Introvale
| Product NDC: | 0781-5584 |
| Proprietary Name: | Introvale |
| Non Proprietary Name: | Levonorgestrel and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Levonorgestrel and Ethinyl Estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Introvale
| Product NDC: | 0781-5584 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079064 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100927 |
Package Information of Introvale
| Package NDC: | 0781-5584-36 |
| Package Description: | 3 CARTON in 1 BOX (0781-5584-36) > 1 KIT in 1 CARTON |
NDC Information of Introvale
| NDC Code | 0781-5584-36 |
| Proprietary Name | Introvale |
| Package Description | 3 CARTON in 1 BOX (0781-5584-36) > 1 KIT in 1 CARTON |
| Product NDC | 0781-5584 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levonorgestrel and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20100927 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
