junel fe 1/20
Generic: norethindrone acetate and ethinyl estradiol, and ferrous fumarate
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
junel fe 1/20
Generic Name
norethindrone acetate and ethinyl estradiol, and ferrous fumarate
Labeler
preferred pharmaceuticals inc.
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
68788-6832
Product ID
68788-6832_01765aa5-7e4e-45b9-bd18-3c692c36c958
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076081
Listing Expiration
2027-12-31
Marketing Start
2016-11-21
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687886832
Hyphenated Format
68788-6832
Supplemental Identifiers
RxCUI
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
junel fe 1/20 (source: ndc)
Generic Name
norethindrone acetate and ethinyl estradiol, and ferrous fumarate (source: ndc)
Application Number
ANDA076081 (source: ndc)
Resolved Composition
Strengths
- 1 mg
- 20 mcg
- 75 mg
Packaging
- 6 BLISTER PACK in 1 CARTON (68788-6832-2) / 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": "01765aa5-7e4e-45b9-bd18-3c692c36c958", "openfda": {"rxcui": ["259176", "1358762", "1358763", "1358765"], "spl_set_id": ["75bb0024-8f1a-4036-9acd-006ea430f3b7"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 BLISTER PACK in 1 CARTON (68788-6832-2) / 1 KIT in 1 BLISTER PACK", "package_ndc": "68788-6832-2", "marketing_start_date": "20161121"}], "brand_name": "Junel Fe 1/20", "product_id": "68788-6832_01765aa5-7e4e-45b9-bd18-3c692c36c958", "dosage_form": "KIT", "product_ndc": "68788-6832", "generic_name": "norethindrone acetate and ethinyl estradiol, and ferrous fumarate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Junel Fe 1/20", "application_number": "ANDA076081", "marketing_category": "ANDA", "marketing_start_date": "20161121", "listing_expiration_date": "20271231"}