iclevia
Generic: levonorgestrel and ethinyl estradiol
Labeler: aurobindo pharma limitedDrug Facts
Product Profile
Brand Name
iclevia
Generic Name
levonorgestrel and ethinyl estradiol
Labeler
aurobindo pharma limited
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
65862-865
Product ID
65862-865_e44389c6-fdd2-408e-8bfe-324842c36d76
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206850
Listing Expiration
2026-12-31
Marketing Start
2018-06-29
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65862865
Hyphenated Format
65862-865
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
iclevia (source: ndc)
Generic Name
levonorgestrel and ethinyl estradiol (source: ndc)
Application Number
ANDA206850 (source: ndc)
Resolved Composition
Strengths
- 0.15 mg
- 0.03 mg
Packaging
- 3 POUCH in 1 CARTON (65862-865-83) / 1 BLISTER PACK in 1 POUCH (65862-865-94) / 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": "e44389c6-fdd2-408e-8bfe-324842c36d76", "openfda": {"rxcui": ["238019", "748797", "751901", "2049264"], "spl_set_id": ["00657f4e-9df8-4f58-91a0-eff5a467f988"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 CARTON (65862-865-83) / 1 BLISTER PACK in 1 POUCH (65862-865-94) / 1 KIT in 1 BLISTER PACK", "package_ndc": "65862-865-83", "marketing_start_date": "20180629"}], "brand_name": "Iclevia", "product_id": "65862-865_e44389c6-fdd2-408e-8bfe-324842c36d76", "dosage_form": "KIT", "product_ndc": "65862-865", "generic_name": "Levonorgestrel and Ethinyl Estradiol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Iclevia", "application_number": "ANDA206850", "marketing_category": "ANDA", "marketing_start_date": "20180629", "listing_expiration_date": "20261231"}