Acarbose
- Product NDC
- 47781-340
- 11-digit product format
- 477810340
- Labeler code
- 47781
- Product ID
- 47781-340_3406d658-a09f-00c1-abba-9a7a8a29786d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acarbose
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Alvogen, Inc.
- Application
- NDA020482
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2008-01-30
- Marketing end
- 2021-12-31
- Substance
- ACARBOSE
- Active strength
- 25 mg/1
- Pharmacologic classes
- alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 47781-340-01 | 47781034001 | 100 TABLET in 1 BOTTLE (47781-340-01) | 100 tablet | 2015-03-12 | 2021-12-31 | No | No | Current |