Alogliptin
- Product NDC
- 50090-5574
- 11-digit product format
- 500905574
- Labeler code
- 50090
- Product ID
- 50090-5574_b2747bb4-79a6-4e24-aa7c-79fe610523e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alogliptin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA022271
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-04-08
- Substance
- ALOGLIPTIN BENZOATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Dipeptidyl Peptidase 4 Inhibitor [EPC], Dipeptidyl Peptidase 4 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Alogliptin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALOGLIPTIN BENZOATE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | EEN99869SC |
| Rxcui | 1368006 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-5574-0 | Alogliptin | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5574 | ALOGLIPTIN TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 6 | Current NDC, Legacy NDC, 1 package rows | 20231025_38d30e4f-4212-4f7a-96b5-74b277b56cba.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5574-0 | 50090557400 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-5574-0) | 2021-07-02 | 0000-00-00 | No | No | Current |