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Campral
Campral - 0456-3330-01 - (acamprosate calcium)
Drug Information of Campral
| Product NDC: | 0456-3330 |
| Proprietary Name: | Campral |
| Non Proprietary Name: | acamprosate calcium |
| Active Ingredient(s): | 333 mg/1 & nbsp; acamprosate calcium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Campral
| Product NDC: | 0456-3330 |
| Labeler Name: | Forest Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021431 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050111 |
Package Information of Campral
| Package NDC: | 0456-3330-01 |
| Package Description: | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (0456-3330-01) |
NDC Information of Campral
| NDC Code | 0456-3330-01 |
| Proprietary Name | Campral |
| Package Description | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (0456-3330-01) |
| Product NDC | 0456-3330 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acamprosate calcium |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20050111 |
| Marketing Category Name | NDA |
| Labeler Name | Forest Laboratories, Inc. |
| Substance Name | ACAMPROSATE CALCIUM |
| Strength Number | 333 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
