Acamprosate Calcium
- Product NDC
- 51079-241
- 11-digit product format
- 510790241
- Labeler code
- 51079
- Product ID
- 51079-241_a75bcba8-c39f-0573-e053-2a95a90a181a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acamprosate calcium enteric-coated
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA200142
- Marketing category
- ANDA
- Marketing start
- 2013-07-16
- Marketing end
- 2021-04-30
- Substance
- ACAMPROSATE CALCIUM
- Active strength
- 333 mg/1
- 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 |
|---|
| 51079-241-06 | 51079024106 | 50 BLISTER PACK in 1 CARTON (51079-241-06) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (51079-241-01) | 50 blister pack | 2013-07-16 | 2021-04-30 | No | No | Current |