Entacapone
- Product NDC
- 51079-273
- 11-digit product format
- 510790273
- Labeler code
- 51079
- Product ID
- 51079-273_d116b620-ea7f-2d98-e053-2995a90a103e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Entacapone
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- NDA020796
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2013-12-12
- Marketing end
- 2022-08-31
- Substance
- ENTACAPONE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Catechol O-Methyltransferase Inhibitors [MoA],Catechol-O-Methyltransferase 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 |
|---|
| 51079-273-03 | 51079027303 | 30 BLISTER PACK in 1 CARTON (51079-273-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-273-01) | 30 blister pack | 2013-12-12 | 0000-00-00 | No | No | Current |