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Daysee - 68180-846-13 - (LEVONORGESTREL AND ETHINYL ESTRADIOL)
Drug Information of Daysee
| Product NDC: | 68180-846 |
| Proprietary Name: | Daysee |
| 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 Daysee
| Product NDC: | 68180-846 |
| Labeler Name: | Lupin Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091467 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130410 |
Package Information of Daysee
| Package NDC: | 68180-846-13 |
| Package Description: | 2 POUCH in 1 CARTON (68180-846-13) > 1 BLISTER PACK in 1 POUCH (68180-846-11) > 1 KIT in 1 BLISTER PACK |
NDC Information of Daysee
| NDC Code | 68180-846-13 |
| Proprietary Name | Daysee |
| Package Description | 2 POUCH in 1 CARTON (68180-846-13) > 1 BLISTER PACK in 1 POUCH (68180-846-11) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 68180-846 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LEVONORGESTREL AND ETHINYL ESTRADIOL |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130410 |
| Marketing Category Name | ANDA |
| Labeler Name | Lupin Pharmaceuticals, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
