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OCELLA
OCELLA - 0555-9131-67 - (drospirenone and ethinyl estradiol)
Drug Information of OCELLA
| Product NDC: | 0555-9131 |
| Proprietary Name: | OCELLA |
| Non Proprietary Name: | drospirenone and ethinyl estradiol |
| Active Ingredient(s): | & nbsp; drospirenone and ethinyl estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OCELLA
| Product NDC: | 0555-9131 |
| Labeler Name: | BARR LABORATORIES, INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021098 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20010611 |
Package Information of OCELLA
| Package NDC: | 0555-9131-67 |
| Package Description: | 3 BLISTER PACK in 1 PACKAGE (0555-9131-67) > 1 KIT in 1 BLISTER PACK (0555-9131-79) |
NDC Information of OCELLA
| NDC Code | 0555-9131-67 |
| Proprietary Name | OCELLA |
| Package Description | 3 BLISTER PACK in 1 PACKAGE (0555-9131-67) > 1 KIT in 1 BLISTER PACK (0555-9131-79) |
| Product NDC | 0555-9131 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | drospirenone and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20010611 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | BARR LABORATORIES, INC. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
