Cimetidine
- Product NDC
- 68788-9064
- 11-digit product format
- 687889064
- Labeler code
- 68788
- Product ID
- 68788-9064_28350d44-360c-421c-b529-a7b03a2a6eea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cimetidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA074151
- Marketing category
- ANDA
- Marketing start
- 2011-07-06
- Marketing end
- 0000-00-00
- Substance
- CIMETIDINE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record