norethindrone
Generic: norethindrone
Labeler: mylan pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
norethindrone
Generic Name
norethindrone
Labeler
mylan pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
norethindrone .35 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0378-7272
Product ID
0378-7272_86deb6b8-705c-4086-bded-e8eff7306208
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200980
Marketing Start
2013-06-24
Marketing End
2026-05-31
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03787272
Hyphenated Format
0378-7272
Supplemental Identifiers
RxCUI
UNII
NUI
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
norethindrone (source: ndc)
Generic Name
norethindrone (source: ndc)
Application Number
ANDA200980 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .35 mg/1
Packaging
- 3 POUCH in 1 CARTON (0378-7272-53) / 1 BLISTER PACK in 1 POUCH (0378-7272-85) / 28 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "86deb6b8-705c-4086-bded-e8eff7306208", "openfda": {"nui": ["M0447349", "N0000175602"], "unii": ["T18F433X4S"], "rxcui": ["198042", "748961"], "spl_set_id": ["8d81169e-63ef-4454-b203-561db1e4bf33"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_epc": ["Progestin [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 CARTON (0378-7272-53) / 1 BLISTER PACK in 1 POUCH (0378-7272-85) / 28 TABLET in 1 BLISTER PACK", "package_ndc": "0378-7272-53", "marketing_end_date": "20260531", "marketing_start_date": "20130624"}], "brand_name": "Norethindrone", "product_id": "0378-7272_86deb6b8-705c-4086-bded-e8eff7306208", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "0378-7272", "generic_name": "Norethindrone", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norethindrone", "active_ingredients": [{"name": "NORETHINDRONE", "strength": ".35 mg/1"}], "application_number": "ANDA200980", "marketing_category": "ANDA", "marketing_end_date": "20260531", "marketing_start_date": "20130624"}