nortrel 7/7/7 (28 day regimen)

Generic: norethindrone and ethinyl estradiol

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nortrel 7/7/7 (28 day regimen)
Generic Name norethindrone and ethinyl estradiol
Labeler proficient rx lp
Dosage Form KIT
Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-685
Product ID 71205-685_5b684f8f-9610-4449-a213-f70bb4a04b8b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075478
Listing Expiration 2026-12-31
Marketing Start 2003-01-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205685
Hyphenated Format 71205-685

Supplemental Identifiers

RxCUI
310463 312033 392662 748797 749852 762007
UPC
0371205685287

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 nortrel 7/7/7 (28 day regimen) (source: ndc)
Generic Name norethindrone and ethinyl estradiol (source: ndc)
Application Number ANDA075478 (source: ndc)

Resolved Composition

Strengths
  • 0.035 mg
  • 0.5 mg
  • 0.75 mg
  • 1 mg
source: label
Packaging
  • 1 BLISTER PACK in 1 POUCH (71205-685-28) / 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": "5b684f8f-9610-4449-a213-f70bb4a04b8b", "openfda": {"upc": ["0371205685287"], "rxcui": ["310463", "312033", "392662", "748797", "749852", "762007"], "spl_set_id": ["5b684f8f-9610-4449-a213-f70bb4a04b8b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 POUCH (71205-685-28)  / 1 KIT in 1 BLISTER PACK", "package_ndc": "71205-685-28", "marketing_start_date": "20220812"}], "brand_name": "Nortrel 7/7/7 (28 Day Regimen)", "product_id": "71205-685_5b684f8f-9610-4449-a213-f70bb4a04b8b", "dosage_form": "KIT", "product_ndc": "71205-685", "generic_name": "Norethindrone and Ethinyl Estradiol", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nortrel 7/7/7", "brand_name_suffix": "(28 Day Regimen)", "application_number": "ANDA075478", "marketing_category": "ANDA", "marketing_start_date": "20030102", "listing_expiration_date": "20261231"}