drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium
Generic: drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium
Labeler: sandoz incDrug Facts
Product Profile
Brand Name
drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium
Generic Name
drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium
Labeler
sandoz inc
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
0781-4103
Product ID
0781-4103_6471e7a9-16b1-4b84-a113-fe6ac0ca5640
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA022574
Listing Expiration
2027-12-31
Marketing Start
2015-08-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07814103
Hyphenated Format
0781-4103
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
drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium (source: ndc)
Generic Name
drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium (source: ndc)
Application Number
NDA022574 (source: ndc)
Resolved Composition
Strengths
- 3 mg
- 0.03 mg
- 0.451 mg
Packaging
- 3 BLISTER PACK in 1 PACKAGE (0781-4103-15) / 1 KIT in 1 BLISTER PACK (0781-4103-52)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "6471e7a9-16b1-4b84-a113-fe6ac0ca5640", "openfda": {"rxcui": ["1013628", "1050492", "1050493"], "spl_set_id": ["6928f186-190d-4c40-beab-81cf80cd45cb"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 PACKAGE (0781-4103-15) / 1 KIT in 1 BLISTER PACK (0781-4103-52)", "package_ndc": "0781-4103-15", "marketing_start_date": "20150801"}], "brand_name": "Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium", "product_id": "0781-4103_6471e7a9-16b1-4b84-a113-fe6ac0ca5640", "dosage_form": "KIT", "product_ndc": "0781-4103", "generic_name": "Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Drospirenone/ethinyl estradiol/levomefolate calcium and levomefolate calcium", "application_number": "NDA022574", "marketing_category": "NDA", "marketing_start_date": "20150801", "listing_expiration_date": "20271231"}