Ranitidine
- Product NDC
- 0781-6087
- 11-digit product format
- 007816087
- Labeler code
- 0781
- Product ID
- 0781-6087_c08234ca-78f9-4e97-a4d4-0fbc4fd45bd1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- SYRUP
- Route
- TOPICAL
- Labeler
- Sandoz Inc.
- Application
- ANDA090054
- Marketing category
- ANDA
- Marketing start
- 2011-10-25
- Marketing end
- 2020-10-25
- Substance
- RANITIDINE
- Active strength
- 15 mg/mL
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record