primaquine phosphate

Generic: primaquine phosphate

Labeler: sanofi-aventis u.s. llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name primaquine phosphate
Generic Name primaquine phosphate
Labeler sanofi-aventis u.s. llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

primaquine phosphate 15 mg/1

Manufacturer
Sanofi-Aventis U.S. LLC

Identifiers & Regulatory

Product NDC 0024-1596
Product ID 0024-1596_7e15f87d-f34f-4ec2-9da8-a041db792623
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA008316
Listing Expiration 2027-12-31
Marketing Start 2011-04-15

Pharmacologic Class

Classes
antimalarial [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00241596
Hyphenated Format 0024-1596

Supplemental Identifiers

RxCUI
904170
UNII
H0982HF78B

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 primaquine phosphate (source: ndc)
Generic Name primaquine phosphate (source: ndc)
Application Number NDA008316 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0024-1596-01)
source: ndc

Packages (1)

0024-1596-01 100 TABLET, FILM COATED in 1 BOTTLE (0024-1596-01)

Ingredients (1)

primaquine phosphate (15 mg/1)

Linked Drug Pages (1)

Primaquine Phosphate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7e15f87d-f34f-4ec2-9da8-a041db792623", "openfda": {"unii": ["H0982HF78B"], "rxcui": ["904170"], "spl_set_id": ["1bfbf4ae-81b8-4160-a00d-6322aadd4b59"], "manufacturer_name": ["Sanofi-Aventis U.S. LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0024-1596-01)", "package_ndc": "0024-1596-01", "marketing_start_date": "20110415"}], "brand_name": "Primaquine Phosphate", "product_id": "0024-1596_7e15f87d-f34f-4ec2-9da8-a041db792623", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "0024-1596", "generic_name": "Primaquine Phosphate", "labeler_name": "Sanofi-Aventis U.S. LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Primaquine Phosphate", "active_ingredients": [{"name": "PRIMAQUINE PHOSPHATE", "strength": "15 mg/1"}], "application_number": "NDA008316", "marketing_category": "NDA", "marketing_start_date": "20110415", "listing_expiration_date": "20271231"}