NDC 0440-8187

Primaquine Phosphate

Primaquine Phosphate

Primaquine Phosphate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Liberty Pharmaceuticals, Inc.. The primary component is Primaquine Phosphate.

Product ID0440-8187_3b38f07f-6737-4f30-8e04-47c3df39e65f
NDC0440-8187
Product TypeHuman Prescription Drug
Proprietary NamePrimaquine Phosphate
Generic NamePrimaquine Phosphate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2014-08-01
Marketing CategoryANDA / ANDA
Application NumberANDA204476
Labeler NameLiberty Pharmaceuticals, Inc.
Substance NamePRIMAQUINE PHOSPHATE
Active Ingredient Strength15 mg/1
Pharm ClassesAntimalarial [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0440-8187-56

56 TABLET in 1 BOTTLE (0440-8187-56)
Marketing Start Date2014-08-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0440-8187-07 [00440818707]

Primaquine Phosphate TABLET
Marketing CategoryANDA
Application NumberANDA204476
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-08-01
Marketing End Date2019-10-15

NDC 0440-8187-28 [00440818728]

Primaquine Phosphate TABLET
Marketing CategoryANDA
Application NumberANDA204476
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-08-01
Marketing End Date2019-10-15

NDC 0440-8187-01 [00440818701]

Primaquine Phosphate TABLET
Marketing CategoryANDA
Application NumberANDA204476
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-08-01
Marketing End Date2019-10-15

NDC 0440-8187-14 [00440818714]

Primaquine Phosphate TABLET
Marketing CategoryANDA
Application NumberANDA204476
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-08-01
Marketing End Date2019-10-15

NDC 0440-8187-56 [00440818756]

Primaquine Phosphate TABLET
Marketing CategoryANDA
Application NumberANDA204476
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-08-01
Marketing End Date2019-10-15

NDC 0440-8187-84 [00440818784]

Primaquine Phosphate TABLET
Marketing CategoryANDA
Application NumberANDA204476
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-08-01
Marketing End Date2019-10-15

Drug Details

Active Ingredients

IngredientStrength
PRIMAQUINE PHOSPHATE15 mg/1

OpenFDA Data

SPL SET ID:acf924c7-37a2-4074-be95-ca9d1f442301
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 904170
  • Pharmacological Class

    • Antimalarial [EPC]

    NDC Crossover Matching brand name "Primaquine Phosphate" or generic name "Primaquine Phosphate"

    NDCBrand NameGeneric Name
    0024-1596Primaquine PhosphatePrimaquine Phosphate
    0440-8187Primaquine PhosphatePrimaquine Phosphate
    33261-671Primaquine PhosphatePrimaquine Phosphate
    42291-510PRIMAQUINE PHOSPHATEPRIMAQUINE PHOSPHATE
    43063-225Primaquine PhosphatePrimaquine Phosphate
    43063-721Primaquine PhosphatePrimaquine Phosphate
    50742-191PRIMAQUINE PHOSPHATEPRIMAQUINE PHOSPHATE
    60429-035Primaquine PhosphatePrimaquine Phosphate
    76385-102Primaquine PhosphatePrimaquine Phosphate

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