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
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 49884-820 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 49884-820 | 49884-820-11 | D | Discontinued by firm | | 2026-07-31 |
Orange Book products#
Application-product, Trade name, Ingredient table| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|
| A206113-001 | ALOSETRON HYDROCHLORIDE | ALOSETRON HYDROCHLORIDE | EQ 0.5MG BASE | TABLET / ORAL | | | 2018-02-23 |
| A206113-002 | ALOSETRON HYDROCHLORIDE | ALOSETRON HYDROCHLORIDE | EQ 1MG BASE | TABLET / ORAL | | | 2018-02-23 |
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 |