Search by Drug Name or NDC
NDC 70518-2887-02 Pravastatin Sodium 20 mg/1 Details
Pravastatin Sodium 20 mg/1
Pravastatin Sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is PRAVASTATIN SODIUM.
Product Information
| NDC | 70518-2887 |
|---|---|
| Product ID | 70518-2887_04dbda97-f40f-846e-e063-6394a90afaf6 |
| 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 | Pravastatin Sodium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Pravastatin Sodium |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | mg/1 |
| Substance Name | PRAVASTATIN SODIUM |
| Labeler Name | REMEDYREPACK INC. |
| Pharmaceutical Class | HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076056 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70518-2887-02 (70518288702)
| NDC Package Code | 70518-2887-2 |
|---|---|
| Billing NDC | 70518288702 |
| Package | 30 TABLET in 1 BLISTER PACK (70518-2887-2) |
| Marketing Start Date | 2022-11-08 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |