levonorgestrel and ethinyl estradiol
Generic: levonorgestrel and ethinyl estradiol
Labeler: glenmark pharmaceuticals inc., usaDrug Facts
Product Profile
Brand Name
levonorgestrel and ethinyl estradiol
Generic Name
levonorgestrel and ethinyl estradiol
Labeler
glenmark pharmaceuticals inc., usa
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
68462-672
Product ID
68462-672_f0db17c7-0387-420c-8ba4-5d0752e5a4ee
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203164
Listing Expiration
2027-12-31
Marketing Start
2015-06-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68462672
Hyphenated Format
68462-672
Supplemental Identifiers
RxCUI
UPC
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
levonorgestrel and ethinyl estradiol (source: ndc)
Generic Name
levonorgestrel and ethinyl estradiol (source: ndc)
Application Number
ANDA203164 (source: ndc)
Resolved Composition
Strengths
- 0.15 mg
- 0.03 mg
- 0.15 mg/0.03 mg
Packaging
- 3 POUCH in 1 CARTON (68462-672-95) / 1 BLISTER PACK in 1 POUCH (68462-672-91) / 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": "f0db17c7-0387-420c-8ba4-5d0752e5a4ee", "openfda": {"upc": ["0368462672952"], "rxcui": ["238019", "748797", "751901"], "spl_set_id": ["3d87d9a4-860a-4ea7-a993-0f4adf1789da"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 CARTON (68462-672-95) / 1 BLISTER PACK in 1 POUCH (68462-672-91) / 1 KIT in 1 BLISTER PACK", "package_ndc": "68462-672-95", "marketing_start_date": "20150612"}], "brand_name": "levonorgestrel and ethinyl estradiol", "product_id": "68462-672_f0db17c7-0387-420c-8ba4-5d0752e5a4ee", "dosage_form": "KIT", "product_ndc": "68462-672", "generic_name": "levonorgestrel and ethinyl estradiol", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levonorgestrel and ethinyl estradiol", "application_number": "ANDA203164", "marketing_category": "ANDA", "marketing_start_date": "20150612", "listing_expiration_date": "20271231"}