granisetron hydrochloride
Generic: granisetron hydrochloride
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
granisetron hydrochloride
Generic Name
granisetron hydrochloride
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
granisetron hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9744
Product ID
0143-9744_3b366664-32e3-4d5c-b75c-0b764ffa31f6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078629
Listing Expiration
2026-12-31
Marketing Start
2009-12-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439744
Hyphenated Format
0143-9744
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
granisetron hydrochloride (source: ndc)
Generic Name
granisetron hydrochloride (source: ndc)
Application Number
ANDA078629 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 VIAL, SINGLE-USE in 1 PACKAGE (0143-9744-10) / 1 mL in 1 VIAL, SINGLE-USE (0143-9744-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3b366664-32e3-4d5c-b75c-0b764ffa31f6", "openfda": {"unii": ["318F6L70J8"], "rxcui": ["240912", "1734399"], "spl_set_id": ["e07862df-f324-4575-a1ef-f7e1cbab4c7a"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 PACKAGE (0143-9744-10) / 1 mL in 1 VIAL, SINGLE-USE (0143-9744-01)", "package_ndc": "0143-9744-10", "marketing_start_date": "20091223"}], "brand_name": "Granisetron Hydrochloride", "product_id": "0143-9744_3b366664-32e3-4d5c-b75c-0b764ffa31f6", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "0143-9744", "generic_name": "Granisetron Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Granisetron Hydrochloride", "active_ingredients": [{"name": "GRANISETRON HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA078629", "marketing_category": "ANDA", "marketing_start_date": "20091223", "listing_expiration_date": "20261231"}