Ranitidine 00121-0727-16

Package NDC

00121-0727-16

Manufacturer: Pharmaceutical Associates, Inc.
Dosage Form: Syrup
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 1, 2010
Listing Expires: December 31, 2026
Application: ANDA077405

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Active Ingredients

Ingredient	Strength
Ranitidine	15 mg/mL

Drug Class

Histamine-2 Receptor Antagonist [EPC]Histamine H2 Receptor Antagonists [MoA]Histamine-2 Receptor Antagonist [EPC]

Selected Package

00121-0727-16Selected

473 mL in 1 BOTTLE (0121-0727-16)