Nizatidine
- Product NDC
- 68788-8913
- 11-digit product format
- 687888913
- Labeler code
- 68788
- Product ID
- 68788-8913_d2d06182-2653-47ea-b96a-08f5700a8970
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nizatidine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090618
- Marketing category
- ANDA
- Marketing start
- 2015-08-28
- Marketing end
- 0000-00-00
- Substance
- NIZATIDINE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record