ocella
Generic: drospirenone and ethinyl estradiol
Labeler: teva pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
ocella
Generic Name
drospirenone and ethinyl estradiol
Labeler
teva pharmaceuticals usa, inc.
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
0555-9131
Product ID
0555-9131_7aced6b3-f763-4234-9b64-2ffdae162347
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA021098
Marketing Start
2001-06-11
Marketing End
2026-06-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05559131
Hyphenated Format
0555-9131
Supplemental Identifiers
RxCUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
ocella (source: ndc)
Generic Name
drospirenone and ethinyl estradiol (source: ndc)
Application Number
NDA021098 (source: ndc)
Resolved Composition
Strengths
- 3 mg
- 0.03 mg
Packaging
- 3 BLISTER PACK in 1 PACKAGE (0555-9131-67) / 1 KIT in 1 BLISTER PACK (0555-9131-79)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "7aced6b3-f763-4234-9b64-2ffdae162347", "openfda": {"rxcui": ["284207", "748797", "748800", "801185"], "spl_set_id": ["0d729f4d-2fa3-47f6-8a1f-d8cfea4cff37"], "manufacturer_name": ["TEVA PHARMACEUTICALS USA, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 PACKAGE (0555-9131-67) / 1 KIT in 1 BLISTER PACK (0555-9131-79)", "package_ndc": "0555-9131-67", "marketing_end_date": "20260630", "marketing_start_date": "20010611"}], "brand_name": "OCELLA", "product_id": "0555-9131_7aced6b3-f763-4234-9b64-2ffdae162347", "dosage_form": "KIT", "product_ndc": "0555-9131", "generic_name": "drospirenone and ethinyl estradiol", "labeler_name": "TEVA PHARMACEUTICALS USA, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OCELLA", "application_number": "NDA021098", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260630", "marketing_start_date": "20010611"}