Metolazone
- Product NDC
- 0615-6501
- 11-digit product format
- 006156501
- Labeler code
- 0615
- Product ID
- 0615-6501_b7334070-8c15-4dee-ae49-8664f3d0f8fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metolazone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA076732
- Marketing category
- ANDA
- Marketing start
- 2003-12-19
- Marketing end
- 0000-00-00
- Substance
- METOLAZONE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide-like Diuretic [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#