errin

Generic: norethindrone

Labeler: mayne pharma inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name errin
Generic Name norethindrone
Labeler mayne pharma inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

norethindrone .35 mg/1

Manufacturer
Mayne Pharma Inc.

Identifiers & Regulatory

Product NDC 51862-886
Product ID 51862-886_b5af3007-e701-4b30-b732-5283b864211f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076225
Listing Expiration 2026-12-31
Marketing Start 2018-04-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51862886
Hyphenated Format 51862-886

Supplemental Identifiers

RxCUI
198042 748961 831533
UNII
T18F433X4S
NUI
M0447349 N0000175602

Packaging Origin

Original Packager
true

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 errin (source: ndc)
Generic Name norethindrone (source: ndc)
Application Number ANDA076225 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .35 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (51862-886-03) / 28 TABLET in 1 BLISTER PACK (51862-886-01)
source: ndc

Packages (1)

Ingredients (1)

norethindrone (.35 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b5af3007-e701-4b30-b732-5283b864211f", "openfda": {"nui": ["M0447349", "N0000175602"], "unii": ["T18F433X4S"], "rxcui": ["198042", "748961", "831533"], "spl_set_id": ["32e6366a-8bb4-4b67-b4a3-e372c7696fa7"], "pharm_class_cs": ["Progesterone Congeners [CS]"], "pharm_class_epc": ["Progestin [EPC]"], "manufacturer_name": ["Mayne Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (51862-886-03)  / 28 TABLET in 1 BLISTER PACK (51862-886-01)", "package_ndc": "51862-886-03", "marketing_start_date": "20180418"}], "brand_name": "ERRIN", "product_id": "51862-886_b5af3007-e701-4b30-b732-5283b864211f", "dosage_form": "TABLET", "pharm_class": ["Progesterone Congeners [CS]", "Progestin [EPC]"], "product_ndc": "51862-886", "generic_name": "NORETHINDRONE", "labeler_name": "Mayne Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ERRIN", "active_ingredients": [{"name": "NORETHINDRONE", "strength": ".35 mg/1"}], "application_number": "ANDA076225", "marketing_category": "ANDA", "marketing_start_date": "20180418", "listing_expiration_date": "20261231"}