Acamprosate Calcium
- Product NDC
- 0093-5352
- 11-digit product format
- 000935352
- Labeler code
- 0093
- Product ID
- 0093-5352_878fe713-bbd5-4ce0-bc48-2c4e9c08655a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acamprosate Calcium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA200143
- Marketing category
- ANDA
- Marketing start
- 2016-03-25
- Marketing end
- 0000-00-00
- Substance
- ACAMPROSATE CALCIUM
- Active strength
- 333 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 0093-5352-86 | 00093535286 | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-5352-86) | 2016-03-25 | 0000-00-00 | No | No | Current |