alosetron hydrochloride

Generic: alosetron hydrochloride

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name alosetron hydrochloride
Generic Name alosetron hydrochloride
Labeler avkare
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

alosetron hydrochloride 1 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 73190-036
Product ID 73190-036_3e64c1e9-713c-8f82-e063-6394a90a7bbb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206647
Listing Expiration 2026-12-31
Marketing Start 2025-07-25

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 73190036
Hyphenated Format 73190-036

Supplemental Identifiers

RxCUI
259306 403975
UPC
0373190036303 0373190035306
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 hydrochloride (source: ndc)
Generic Name alosetron hydrochloride (source: ndc)
Application Number ANDA206647 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (73190-036-30)
source: ndc

Packages (1)

73190-036-30 30 TABLET, FILM COATED in 1 BOTTLE (73190-036-30)

Ingredients (1)

alosetron hydrochloride (1 mg/1)

Linked Drug Pages (1)

Alosetron Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e64c1e9-713c-8f82-e063-6394a90a7bbb", "openfda": {"upc": ["0373190036303", "0373190035306"], "unii": ["2F5R1A46YW"], "rxcui": ["259306", "403975"], "spl_set_id": ["3ac203a2-4c55-deac-e063-6394a90aa165"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (73190-036-30)", "package_ndc": "73190-036-30", "marketing_start_date": "20250725"}], "brand_name": "Alosetron Hydrochloride", "product_id": "73190-036_3e64c1e9-713c-8f82-e063-6394a90a7bbb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "73190-036", "generic_name": "Alosetron Hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alosetron Hydrochloride", "active_ingredients": [{"name": "ALOSETRON HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA206647", "marketing_category": "ANDA", "marketing_start_date": "20250725", "listing_expiration_date": "20261231"}