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Oracit
Oracit - 55154-7352-5 - (Oral Citrate)
Drug Information of Oracit
| Product NDC: | 55154-7352 |
| Proprietary Name: | Oracit |
| Non Proprietary Name: | Oral Citrate |
| Active Ingredient(s): | 490; 640 mg/5mL; mg/5mL & nbsp; Oral Citrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oracit
| Product NDC: | 55154-7352 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110607 |
Package Information of Oracit
| Package NDC: | 55154-7352-5 |
| Package Description: | 5 BOTTLE in 1 BAG (55154-7352-5) > 15 mL in 1 BOTTLE |
NDC Information of Oracit
| NDC Code | 55154-7352-5 |
| Proprietary Name | Oracit |
| Package Description | 5 BOTTLE in 1 BAG (55154-7352-5) > 15 mL in 1 BOTTLE |
| Product NDC | 55154-7352 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Oral Citrate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110607 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cardinal Health |
| Substance Name | CITRIC ACID MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE |
| Strength Number | 490; 640 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
