Glipizide
- Product NDC
- 50436-0908
- 11-digit product format
- 504360908
- Labeler code
- 50436
- Product ID
- 50436-0908_9e0d7c95-4bf8-4f9e-85bf-add84a9b5d55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Glipizide
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA076467
- Marketing category
- ANDA
- Marketing start
- 2006-04-03
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0908-1 | GlipizideER | 30 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0908 | GLIPIZIDE ER (GLIPIZIDE) TABLET, FILM COATED, EXTENDED RELEASE [UNIT DOSE SERVICES] | 4 | Legacy NDC, 1 package rows | 20171109_8b38ed9c-1f9c-4059-9ee2-6a56cb0fcaa3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0908-1 | 50436090801 | 30 in 1 BOTTLE | Historical |