ACITRETIN
- Product NDC
- 66993-896
- 11-digit product format
- 669930896
- Labeler code
- 66993
- Product ID
- 66993-896_93859f30-5f22-44bd-8adc-b9570b1110d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acitretin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Application
- NDA019821
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2013-07-19
- Marketing end
- 2022-04-03
- Substance
- ACITRETIN
- Active strength
- 25 mg/1
- Pharmacologic classes
- Retinoid [EPC],Retinoids [CS]
- 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 |
|---|
| 66993-896-30 | 66993089630 | 30 CAPSULE in 1 BOTTLE (66993-896-30) | 30 capsule | 2013-07-19 | 2022-04-03 | No | No | Current |