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NDC 70756-0250-90 Atorvastatin calcium 80 mg/1 Details
Atorvastatin calcium 80 mg/1
Atorvastatin calcium is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lifestar Pharma LLC. The primary component is ATORVASTATIN CALCIUM TRIHYDRATE.
Product Information
| NDC | 70756-0250 |
|---|---|
| Product ID | 70756-250_96f45871-7175-49d8-8374-dfa2978d38c7 |
| 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 | Atorvastatin calcium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Atorvastatin calcium |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 80 |
| Active Ingredient Units | mg/1 |
| Substance Name | ATORVASTATIN CALCIUM TRIHYDRATE |
| Labeler Name | Lifestar Pharma LLC |
| Pharmaceutical Class | HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA217081 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 70756-0250-90 (70756025090)
| NDC Package Code | 70756-250-90 |
|---|---|
| Billing NDC | 70756025090 |
| Package | 90 TABLET, FILM COATED in 1 BOTTLE (70756-250-90) |
| Marketing Start Date | 2024-01-05 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |