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) |
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 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 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 | |
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