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Triazolam - Medication Information

Product NDC Code 70771-1576
Drug Name

Triazolam

Type Generic
Pharm Class Benzodiazepine [EPC],
Benzodiazepines [CS]
Active Ingredients
Triazolam .125 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 198317,
198318
Application Number ANDA213003
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1576-1 100 tablet in 1 bottle (70771-1576-1)
70771-1576-5 500 tablet in 1 bottle (70771-1576-5)
70771-1576-8 10 tablet in 1 bottle (70771-1576-8)
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Spl product data elements

Usually a list of ingredients in a drug product.
Triazolam Triazolam TRIAZOLAM TRIAZOLAM D&C RED NO. 27 FD&C BLUE NO. 1 LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POVIDONE SILICON DIOXIDE SODIUM LAURYL SULFATE STARCH, CORN light-grayish blue elliptical 12;89 Triazolam Triazolam TRIAZOLAM TRIAZOLAM LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POVIDONE SILICON DIOXIDE SODIUM LAURYL SULFATE STARCH, CORN off-white elliptical 1521

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1576-8 Triazolam Tablets USP, 0.125 mg 10 Tablets Rx only NDC 70771-1162- 8 Triazolam Tablets USP, 0.25 mg 10 Tablets Rx only 0.125 mg label 0.25 mg label

Spl medguide

Information about the patient medication guide that accompanies the drug product. Certain drugs must be dispensed with an accompanying medication guide. This field may contain information about when to consult the medication guide and the contents of the medication guide.
SPL MEDGUIDE

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API