ALOSETRON HYDROCHLORIDE
- Product NDC
- 49884-820
- 11-digit product format
- 498840820
- Labeler code
- 49884
- Product ID
- 49884-820_7382cc38-ca25-4aa6-af5d-4b52fd1eec7b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALOSETRON HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA206113
- Marketing category
- ANDA
- Marketing start
- 2019-04-05
- Marketing end
- 0000-00-00
- Substance
- ALOSETRON HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 49884-820-11 | 49884082011 | 30 TABLET in 1 BOTTLE (49884-820-11) | 30 tablet | 2019-04-05 | 0000-00-00 | No | No | Current |