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Zinga Brand names, Zinga Analogs

Zinga Brand Names Mixture

  • No information avaliable

Zinga Chemical_Formula


Zinga RX_link


Zinga fda sheet

Zinga FDA

Zinga msds (material safety sheet)

Zinga Synthesis Reference

R. P. Pioch, U.S. Pat. 4,375,547 (1982)

Zinga Molecular Weight

331.46 g/mol

Zinga Melting Point

203 oC

Zinga H2O Solubility


Zinga State


Zinga LogP


Zinga Dosage Forms

Capsule (150, 300 mg)

Zinga Indication

For the treatment of acid-reflux disorders (GERD), peptic ulcer disease, active benign gastric ulcer, and active duodenal ulcer.

Zinga Pharmacology

Nizatidine is a competitive, reversible inhibitor of histamine at the histamine H2-receptors, particularly those in the gastric parietal cells. By inhibiting the action of histamine on stomach cells, nizatidine reduces stomach acid production. Nizatidine had no demonstrable antiandrogenic action. Full-dose therapy for the problems treated by nizatidine lasts no longer than 8 weeks. It has been demonstrated that treatment with a reduced dose of nizatidine is effective as maintenance therapy following healing of active duodenal ulcers.

Zinga Absorption

Rapid (bioavailability of nizatidine exceeds 70%)

Zinga side effects and Toxicity

Oral, rat LD50: 301 mg/kg. Symptoms of overdose include cholinergic-type effects including lacrimation, salivation, emesis, miosis, and diarrhea.

Zinga Patient Information

Zinga Organisms Affected

Humans and other mammals