66220-719 : Kristalose 10 g/10g Oral Powder, for Solution


NDC: 66220-719
Labeler: Cumberland Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name:  Kristalose
Dosage Form: Oral Powder, for Solution
Application #: ANDA074712
Rev. Date: 


NDC Package Codes:

  • 66220-719-30: 30 POUCH IN 1 CARTON (66220‑719‑30) > 10 G IN 1 POUCH (66220‑719‑01)

Active Ingredients:

  • Lactulose

Dosage Strength:

  • 10 g/10g

Pharmaceutical Classes:

  • Osmotic Laxative [EPC]
  • Osmotic Activity [MoA]
  • Acidifying Activity [MoA]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Related Products:

Based on records with the same trade name.
  • 66220-729 Kristalose 20 g/20g Oral Powder, for Solution by Cumberland Pharmaceuticals Inc.
  • 67414-719 Kristalose 10 g/10g Oral Powder, for Solution by Jones Contract Packaging Services
  • 67414-729 Kristalose 20 g/20g Oral Powder, for Solution by Jones Contract Packaging Services

NDC QR Code

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NDC 66220-719 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.