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Estarylla
Estarylla - 0781-4058-15 - (Norgestimate and ethinyl estradiol)
Drug Information of Estarylla
| Product NDC: | 0781-4058 |
| Proprietary Name: | Estarylla |
| Non Proprietary Name: | Norgestimate and ethinyl estradiol |
| Active Ingredient(s): | & nbsp; Norgestimate and ethinyl estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Estarylla
| Product NDC: | 0781-4058 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090794 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130201 |
Package Information of Estarylla
| Package NDC: | 0781-4058-15 |
| Package Description: | 3 BLISTER PACK in 1 BOX (0781-4058-15) > 1 KIT in 1 BLISTER PACK |
NDC Information of Estarylla
| NDC Code | 0781-4058-15 |
| Proprietary Name | Estarylla |
| Package Description | 3 BLISTER PACK in 1 BOX (0781-4058-15) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 0781-4058 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norgestimate and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130201 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
