Tolcapone
- Product NDC
- 49884-254
- 11-digit product format
- 498840254
- Labeler code
- 49884
- Product ID
- 49884-254_75578ac3-ecaa-4a4e-b7ef-94246a6f3199
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tolcapone
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA204584
- Marketing category
- ANDA
- Marketing start
- 2015-01-06
- Marketing end
- 0000-00-00
- Substance
- TOLCAPONE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Catechol O-Methyltransferase Inhibitors [MoA],Catechol-O-Methyltransferase Inhibitor [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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49884-254-09 | 49884025409 | 90 TABLET, COATED in 1 BOTTLE (49884-254-09) | 2015-01-06 | 0000-00-00 | No | No | Current |