Ranitidine
- Product NDC
- 23155-291
- 11-digit product format
- 231550291
- Labeler code
- 23155
- Product ID
- 23155-291_6bf5f8d4-1a53-499c-8ef8-8b6c7383bc62
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals
- Application
- ANDA090102
- Marketing category
- ANDA
- Marketing start
- 2013-07-15
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDR
- Active strength
- 15 mg/mL
- Pharmacologic classes
- Histamine H2 Re
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record