Acarbose
- Product NDC
- 50090-4952
- 11-digit product format
- 500904952
- Labeler code
- 50090
- Product ID
- 50090-4952_b1bcf2a4-293e-4345-afab-95db4588384f
- 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
- 50 mg/1
- Pharmacologic classes
- alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4952-1 | 50090495201 | 30 TABLET in 1 BOTTLE (50090-4952-1) | 30 tablet | 2020-03-03 | 0000-00-00 | No | No | Current |