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NDC 65197-0420-60 Emetrol Chewables Mixed Berry 230 mg/1 Details
Emetrol Chewables Mixed Berry 230 mg/1
Emetrol Chewables Mixed Berry is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by WellSpring Pharmaceutical Corporation. The primary component is TRISODIUM CITRATE DIHYDRATE.
Product Information
| NDC | 65197-0420 |
|---|---|
| Product ID | 65197-420_9b0e4c82-36af-43f9-84e2-98a58aee0319 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Emetrol Chewables Mixed Berry |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Sodium citrate dihydrate |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, CHEWABLE |
| Route | ORAL |
| Active Ingredient Strength | 230 |
| Active Ingredient Units | mg/1 |
| Substance Name | TRISODIUM CITRATE DIHYDRATE |
| Labeler Name | WellSpring Pharmaceutical Corporation |
| Pharmaceutical Class | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE] |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 65197-0420-60 (65197042060)
| NDC Package Code | 65197-420-60 |
|---|---|
| Billing NDC | 65197042060 |
| Package | 1 BOTTLE in 1 BOX (65197-420-60) / 60 TABLET, CHEWABLE in 1 BOTTLE |
| Marketing Start Date | 2023-07-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |