nora be
Generic: norethindrone
Labeler: actavis pharma, inc.Drug Facts
Product Profile
Brand Name
nora be
Generic Name
norethindrone
Labeler
actavis pharma, inc.
Dosage Form
TABLET
Routes
Active Ingredients
norethindrone .35 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
52544-629
Product ID
52544-629_d98a1fdf-3727-41aa-9974-9a7680441740
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA017060
Marketing Start
2005-05-12
Marketing End
2026-06-30
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
52544629
Hyphenated Format
52544-629
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
nora be (source: ndc)
Generic Name
norethindrone (source: ndc)
Application Number
NDA017060 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .35 mg/1
Packaging
- 6 PACKAGE in 1 CARTON (52544-629-28) / 28 TABLET in 1 PACKAGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d98a1fdf-3727-41aa-9974-9a7680441740", "openfda": {"nui": ["M0447349", "N0000175602"], "unii": ["T18F433X4S"], "rxcui": ["198042", "748961", "748977"], "spl_set_id": ["a9241f0b-e1d0-4782-98e6-7f1eaf9ccc85"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_epc": ["Progestin [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 PACKAGE in 1 CARTON (52544-629-28) / 28 TABLET in 1 PACKAGE", "package_ndc": "52544-629-28", "marketing_end_date": "20260630", "marketing_start_date": "20050512"}], "brand_name": "Nora BE", "product_id": "52544-629_d98a1fdf-3727-41aa-9974-9a7680441740", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "52544-629", "generic_name": "Norethindrone", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nora BE", "active_ingredients": [{"name": "NORETHINDRONE", "strength": ".35 mg/1"}], "application_number": "NDA017060", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260630", "marketing_start_date": "20050512"}