norethindrone

Generic: norethindrone

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name norethindrone
Generic Name norethindrone
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

norethindrone .35 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6161
Product ID 50090-6161_9dc94f9a-0113-49fe-9500-2a96808b9888
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091325
Listing Expiration 2026-12-31
Marketing Start 2020-11-11

Pharmacologic Class

Established (EPC)
progestin [epc]
Chemical Structure
progesterone congeners [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906161
Hyphenated Format 50090-6161

Supplemental Identifiers

RxCUI
198042 748961
UNII
T18F433X4S
NUI
M0447349 N0000175602

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 ANDA091325 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .35 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (50090-6161-0) / 28 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

50090-6161-0 1 BLISTER PACK in 1 CARTON (50090-6161-0) / 28 TABLET in 1 BLISTER PACK

Ingredients (1)

norethindrone (.35 mg/1)

Linked Drug Pages (1)

NORETHINDRONE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9dc94f9a-0113-49fe-9500-2a96808b9888", "openfda": {"nui": ["M0447349", "N0000175602"], "unii": ["T18F433X4S"], "rxcui": ["198042", "748961"], "spl_set_id": ["70231aa1-9dd2-420f-9cb3-432d3c2477d1"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_epc": ["Progestin [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-6161-0)  / 28 TABLET in 1 BLISTER PACK", "package_ndc": "50090-6161-0", "marketing_start_date": "20221011"}], "brand_name": "NORETHINDRONE", "product_id": "50090-6161_9dc94f9a-0113-49fe-9500-2a96808b9888", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "50090-6161", "generic_name": "NORETHINDRONE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NORETHINDRONE", "active_ingredients": [{"name": "NORETHINDRONE", "strength": ".35 mg/1"}], "application_number": "ANDA091325", "marketing_category": "ANDA", "marketing_start_date": "20201111", "listing_expiration_date": "20261231"}