Glipizide
- Product NDC
- 68084-295
- 11-digit product format
- 680840295
- Labeler code
- 68084
- Product ID
- 68084-295_e5d284fc-a71c-a598-e053-2a95a90a539a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA076467
- Marketing category
- ANDA
- Marketing start
- 2008-10-31
- Marketing end
- 2022-11-30
- Substance
- GLIPIZIDE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-295-21 | 68084029521 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-295-21) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-295-11) | 30 blister pack | 2008-10-31 | 0000-00-00 | No | No | Current |