44911-0049 : Anpituapar Oral Liquid


NDC: 44911-0049
Labeler: Energique, Inc.
Product Type: Human Prescription Drug
Drug Name: Anpituapar
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 44911-0049-1: 30 ML IN 1 BOTTLE, DROPPER (44911‑0049‑1)

Active Ingredients:

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

Dosage Strength:

  • 6 [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
  • 12 [hp_X]/mL

Pharmaceutical Classes:

  • Adrenocorticotropic Hormone [CS]
  • Adrenocorticotropic Hormone [EPC]
  • Osmotic Laxative [EPC]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Osmotic Activity [MoA]

Related Products:

Based on records with the same trade name.
  • 44911-0368 Anpituapar Oral Liquid by Energique, Inc.
  • 44911-0526 Anpituapar Oral Liquid by Energique, Inc.

NDC QR Code

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

NDC 44911-0049 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.