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Orsythia
Orsythia - 0603-7634-49 - (levonorgestrel and ethinyl estradiol)
Drug Information of Orsythia
| Product NDC: | 0603-7634 |
| Proprietary Name: | Orsythia |
| Non Proprietary Name: | levonorgestrel and ethinyl estradiol |
| Active Ingredient(s): | & nbsp; levonorgestrel and ethinyl estradiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Orsythia
| Product NDC: | 0603-7634 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077099 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110511 |
Package Information of Orsythia
| Package NDC: | 0603-7634-49 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (0603-7634-49) > 1 KIT in 1 BLISTER PACK (0603-7634-01) * 21 TABLET, FILM COATED in 1 KIT * 7 TABLET, FILM COATED in 1 KIT |
NDC Information of Orsythia
| NDC Code | 0603-7634-49 |
| Proprietary Name | Orsythia |
| Package Description | 3 BLISTER PACK in 1 CARTON (0603-7634-49) > 1 KIT in 1 BLISTER PACK (0603-7634-01) * 21 TABLET, FILM COATED in 1 KIT * 7 TABLET, FILM COATED in 1 KIT |
| Product NDC | 0603-7634 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levonorgestrel and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20110511 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
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