nortrel 7/7/7 (28 day regimen)
Generic: norethindrone and ethinyl estradiol
Labeler: proficient rx lpDrug 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
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
UPC
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
Packaging
- 1 BLISTER PACK in 1 POUCH (71205-685-28) / 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": "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"}