pemetrexed
Generic: pemetrexed
Labeler: solco healthcare us, llcDrug Facts
Product Profile
Brand Name
pemetrexed
Generic Name
pemetrexed
Labeler
solco healthcare us, llc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
pemetrexed disodium hemipentahydrate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43547-632
Product ID
43547-632_b2088b2f-1c23-4bbf-91b3-1fc879180b8f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216582
Listing Expiration
2027-12-31
Marketing Start
2024-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43547632
Hyphenated Format
43547-632
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
pemetrexed (source: ndc)
Generic Name
pemetrexed (source: ndc)
Application Number
ANDA216582 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 100 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (43547-632-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b2088b2f-1c23-4bbf-91b3-1fc879180b8f", "openfda": {"unii": ["F4GSH45R4C"], "rxcui": ["1728077"], "spl_set_id": ["bd0ada98-3237-4465-8ba2-3a12c33116fb"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (43547-632-01)", "package_ndc": "43547-632-01", "marketing_start_date": "20240701"}], "brand_name": "Pemetrexed", "product_id": "43547-632_b2088b2f-1c23-4bbf-91b3-1fc879180b8f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "43547-632", "generic_name": "Pemetrexed", "labeler_name": "Solco Healthcare US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "100 mg/1"}], "application_number": "ANDA216582", "marketing_category": "ANDA", "marketing_start_date": "20240701", "listing_expiration_date": "20271231"}