alosetron

Generic: alosetron

Labeler: lifestar pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alosetron
Generic Name alosetron
Labeler lifestar pharma llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alosetron hydrochloride 1 mg/1

Manufacturer
Lifestar Pharma LLC

Identifiers & Regulatory

Product NDC 70756-701
Product ID 70756-701_6e1e5a99-5018-42e7-8e2c-bcd0ac1e80fb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213614
Listing Expiration 2026-12-31
Marketing Start 2020-09-14

Pharmacologic Class

Classes
serotonin 3 receptor antagonists [moa] serotonin-3 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70756701
Hyphenated Format 70756-701

Supplemental Identifiers

RxCUI
259306 403975
UNII
2F5R1A46YW

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 alosetron (source: ndc)
Generic Name alosetron (source: ndc)
Application Number ANDA213614 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (70756-701-30)
source: ndc

Packages (1)

70756-701-30 30 TABLET in 1 BOTTLE (70756-701-30)

Ingredients (1)

alosetron hydrochloride (1 mg/1)

Linked Drug Pages (1)

Alosetron ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6e1e5a99-5018-42e7-8e2c-bcd0ac1e80fb", "openfda": {"unii": ["2F5R1A46YW"], "rxcui": ["259306", "403975"], "spl_set_id": ["2846a244-7540-442b-81bc-638e641497ce"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (70756-701-30)", "package_ndc": "70756-701-30", "marketing_start_date": "20200914"}], "brand_name": "Alosetron", "product_id": "70756-701_6e1e5a99-5018-42e7-8e2c-bcd0ac1e80fb", "dosage_form": "TABLET", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "70756-701", "generic_name": "Alosetron", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alosetron", "active_ingredients": [{"name": "ALOSETRON HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA213614", "marketing_category": "ANDA", "marketing_start_date": "20200914", "listing_expiration_date": "20261231"}