Famotidine
- Product NDC
- 0615-4594
- 11-digit product format
- 006154594
- Labeler code
- 0615
- Product ID
- 0615-4594_c007c1bf-9f5c-4c09-a5bd-e2346d756998
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA075511
- Marketing category
- ANDA
- Marketing start
- 2010-04-30
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 40 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
FDA-Initiated Inactive NDC Indexing#