daysee
Generic: levonorgestrel and ethinyl estradiol
Labeler: lupin pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
daysee
Generic Name
levonorgestrel and ethinyl estradiol
Labeler
lupin pharmaceuticals, inc.
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
68180-846
Product ID
68180-846_9d52f9d2-f66b-4457-8cb7-c48a6e7d076f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091467
Listing Expiration
2026-12-31
Marketing Start
2013-04-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68180846
Hyphenated Format
68180-846
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
daysee (source: ndc)
Generic Name
levonorgestrel and ethinyl estradiol (source: ndc)
Application Number
ANDA091467 (source: ndc)
Resolved Composition
Strengths
- 0.15 mg
- 0.03 mg
- 0.01 mg
- 0.15 mg/0.03 mg
Packaging
- 2 POUCH in 1 CARTON (68180-846-13) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "9d52f9d2-f66b-4457-8cb7-c48a6e7d076f", "openfda": {"rxcui": ["238019", "248310", "749761", "1423123"], "spl_set_id": ["a9861412-4e54-4984-b14c-a1dd91d5c946"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 POUCH in 1 CARTON (68180-846-13) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK", "package_ndc": "68180-846-13", "marketing_start_date": "20130410"}], "brand_name": "Daysee", "product_id": "68180-846_9d52f9d2-f66b-4457-8cb7-c48a6e7d076f", "dosage_form": "KIT", "product_ndc": "68180-846", "generic_name": "LEVONORGESTREL AND ETHINYL ESTRADIOL", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Daysee", "application_number": "ANDA091467", "marketing_category": "ANDA", "marketing_start_date": "20130410", "listing_expiration_date": "20261231"}