alosetron hydrochloride

Generic: alosetron hydrochloride

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

Drug Facts

Product Profile

Brand Name alosetron hydrochloride
Generic Name alosetron hydrochloride
Labeler eywa pharma inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

alosetron hydrochloride 1 mg/1

Manufacturer
Eywa Pharma Inc

Identifiers & Regulatory

Product NDC 71930-011
Product ID 71930-011_c304be8d-9fa3-4d89-885e-5a6bf1e80a2b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211621
Listing Expiration 2026-12-31
Marketing Start 2019-02-01

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 71930011
Hyphenated Format 71930-011

Supplemental Identifiers

RxCUI
259306 403975
UPC
0371930010309 0371930011306
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 ANDA211621 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71930-011-30)
source: ndc

Packages (1)

71930-011-30 30 TABLET in 1 BOTTLE (71930-011-30)

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": "c304be8d-9fa3-4d89-885e-5a6bf1e80a2b", "openfda": {"upc": ["0371930010309", "0371930011306"], "unii": ["2F5R1A46YW"], "rxcui": ["259306", "403975"], "spl_set_id": ["d62b2c5a-1693-4e67-96d5-197e1fdc8694"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71930-011-30)", "package_ndc": "71930-011-30", "marketing_start_date": "20190201"}], "brand_name": "Alosetron Hydrochloride", "product_id": "71930-011_c304be8d-9fa3-4d89-885e-5a6bf1e80a2b", "dosage_form": "TABLET", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "71930-011", "generic_name": "Alosetron Hydrochloride", "labeler_name": "Eywa Pharma Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alosetron Hydrochloride", "active_ingredients": [{"name": "ALOSETRON HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA211621", "marketing_category": "ANDA", "marketing_start_date": "20190201", "listing_expiration_date": "20261231"}