Acarbose
- Product NDC
- 50090-5829
- 11-digit product format
- 500905829
- Labeler code
- 50090
- Product ID
- 50090-5829_49410201-806b-4f8b-9638-24f91d5ae72b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acarbose
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090912
- Marketing category
- ANDA
- Marketing start
- 2016-12-10
- Marketing end
- 0000-00-00
- Substance
- ACARBOSE
- Active strength
- 100 mg/1
- Pharmacologic classes
- alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-5829-0 | Acarbose | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5829 | ACARBOSE TABLET [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 1 package rows | 20211030_bf8500e1-9037-43f5-855b-d336d92d5cb7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5829-0 | 50090582900 | 30 TABLET in 1 BOTTLE (50090-5829-0) | 30 tablet | 2021-10-26 | 0000-00-00 | No | No | Current |