junel fe 1/20

Generic: norethindrone acetate and ethinyl estradiol, and ferrous fumarate

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

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
Preferred Pharmaceuticals Inc.

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
259176 1358762 1358763 1358765

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
source: label
Packaging
  • 6 BLISTER PACK in 1 CARTON (68788-6832-2) / 1 KIT in 1 BLISTER PACK
source: ndc

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"}