primaquine phosphate

Generic: primaquine phosphate

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name primaquine phosphate
Generic Name primaquine phosphate
Labeler avkare
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

primaquine phosphate 15 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 42291-510
Product ID 42291-510_4ba945a5-47a2-e791-e063-6294a90a9f8a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206043
Listing Expiration 2027-12-31
Marketing Start 2019-02-21

Pharmacologic Class

Classes
antimalarial [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42291510
Hyphenated Format 42291-510

Supplemental Identifiers

RxCUI
904170
UNII
H0982HF78B

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 ANDA206043 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (42291-510-01)
source: ndc

Packages (1)

Ingredients (1)

primaquine phosphate (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ba945a5-47a2-e791-e063-6294a90a9f8a", "openfda": {"unii": ["H0982HF78B"], "rxcui": ["904170"], "spl_set_id": ["82465385-4602-7f46-e053-2991aa0a9fdf"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42291-510-01)", "package_ndc": "42291-510-01", "marketing_start_date": "20190221"}], "brand_name": "PRIMAQUINE PHOSPHATE", "product_id": "42291-510_4ba945a5-47a2-e791-e063-6294a90a9f8a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]"], "product_ndc": "42291-510", "generic_name": "PRIMAQUINE PHOSPHATE", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRIMAQUINE PHOSPHATE", "active_ingredients": [{"name": "PRIMAQUINE PHOSPHATE", "strength": "15 mg/1"}], "application_number": "ANDA206043", "marketing_category": "ANDA", "marketing_start_date": "20190221", "listing_expiration_date": "20271231"}