Glipizide
- Product NDC
- 0615-5585
- 11-digit product format
- 006155585
- Labeler code
- 0615
- Product ID
- 0615-5585_04f7ce27-0809-4974-9850-7d1c10dd1ad5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA076467
- Marketing category
- ANDA
- Marketing start
- 2003-09-08
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#