Acamprosate Calcium
- Product NDC
- 42291-104
- 11-digit product format
- 422910104
- Labeler code
- 42291
- Product ID
- 42291-104_d579615f-15b1-2294-e053-2a95a90a44ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acamprosate Calcium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA200143
- Marketing category
- ANDA
- Marketing start
- 2016-05-16
- Marketing end
- 0000-00-00
- Substance
- ACAMPROSATE CALCIUM
- Active strength
- 333 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 42291-104-18 | 42291010418 | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (42291-104-18) | 2016-05-16 | 0000-00-00 | No | No | Current |