GLIPIZIDE ER
- Product NDC
- 72189-070
- 11-digit product format
- 721890070
- Labeler code
- 72189
- Product ID
- 72189-070_a825166c-fac3-06b1-e053-2995a90a58cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA076467
- Marketing category
- ANDA
- Marketing start
- 2020-06-15
- Marketing end
- 0000-00-00
- Substance
- GLIPIZIDE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-070 | GLIPIZIDE ER (GLIPIZIDE) TABLET, FILM COATED, EXTENDED RELEASE [DIRECT RX] | 2 | Legacy NDC | 20250119_a825166c-fac2-06b1-e053-2995a90a58cf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-070-90 | 72189007090 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-070-90) | 2020-06-15 | 0000-00-00 | No | No | Current |