44911-0526 : Anpituapar Oral Liquid


NDC: 44911-0526
Labeler: Energique, Inc.
Product Type: Human OTC Drug
Drug Name: Anpituapar
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 44911-0526-1: 30 ML IN 1 BOTTLE, DROPPER (44911‑0526‑1)

Active Ingredients:

  • Sus Scrofa Pituitary Gland
  • Chaste Tree Fruit
  • Barium Carbonate
  • Oyster Shell Calcium Carbonate
  • Crude
  • Iodine
  • Sodium Chloride
  • Phosphoric Acid
  • Sepia Officinalis Juice
  • Sus Scrofa Thyroid
  • Canis Lupus Familiaris Milk
  • Corticotropin

Dosage Strength:

  • 8 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 16 [hp_X]/mL
  • 15 [hp_C]/mL

Pharmaceutical Classes:

  • Adrenocorticotropic Hormone [CS]
  • Adrenocorticotropic Hormone [EPC]

Related Products:

Based on records with the same trade name.
  • 44911-0049 Anpituapar Oral Liquid by Energique, Inc.
  • 44911-0368 Anpituapar Oral Liquid by Energique, Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 44911-0526 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.