Prescription drug · ANDA
Atorvastatin calcium NDC 70518-4321
Atorvastatin 40 mg/1 · Tablet · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-4321-0 | 70518432100 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-4321-0)Marketed from Mar 27, 2025 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Atorvastatin calcium
- Generic name (nonproprietary)
- atorvastatin calcium
- Active ingredients
- Atorvastatin — 40 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- REMEDYREPACK INC.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 213853
- Marketing start
- Listing expires
- Other FDA classes
- Hydroxymethylglutaryl-CoA Reductase Inhibitors (Mechanism)
- Identifiers
- Product ID 70518-4321_5aaa777f-0364-6d19-e063-6394a90ad0e7SPL ID 5aaa777f-0364-6d19-e063-6394a90ad0e7SPL set ID 604a011e-6c64-4895-8f6e-d28f119c4c22RxCUI 617311UNII A0JWA85V8F
- Pharmacologic class
- HMG-CoA Reductase Inhibitor
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N470518432100followed by a unit qualifier and the quantityPackage 70518-4321-00. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 213853
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Atorvastatin calcium | Atorvastatin 20 mg/1 | TabletOral | NIVAGEN PHARMACEUTICALS, INC. | 75834-256 |
| Atorvastatin calcium | Atorvastatin 40 mg/1 | TabletOral | NIVAGEN PHARMACEUTICALS, INC. | 75834-257 |
| Atorvastatin calcium | Atorvastatin 80 mg/1 | TabletOral | NIVAGEN PHARMACEUTICALS, INC. | 75834-258 |
| Atorvastatin calcium | Atorvastatin 20 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-2967 |
| Atorvastatin calcium | Atorvastatin 20 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-3783 |
| Atorvastatin calcium | Atorvastatin 10 mg/1 | TabletOral | NIVAGEN PHARMACEUTICALS, INC. | 75834-255 |
| Atorvastatin calcium | Atorvastatin 80 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-3848 |
| Atorvastatin calcium | Atorvastatin 40 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2697 |
| Atorvastatin calcium | Atorvastatin 80 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-9646 |
| Atorvastatin calcium | Atorvastatin 20 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2213 |
| Atorvastatin Calcium | Atorvastatin 10 mg/1 | TabletOral | Direct_Rx | 72189-531 |
| Atorvastatin Calcium | Atorvastatin 20 mg/1 | TabletOral | DirectRX | 72189-291 |
| Atorvastatin calcium | Atorvastatin 40 mg/1 | TabletOral | Proficient Rx LP | 82804-056 |
| Atorvastatin calcium | Atorvastatin 20 mg/1 | TabletOral | Umedica Laboratories USA Inc. | 60290-040 |
| Atorvastatin calcium | Atorvastatin 10 mg/1 | TabletOral | Umedica Laboratories USA Inc. | 60290-039 |
| Atorvastatin calcium | Atorvastatin 80 mg/1 | TabletOral | Umedica Laboratories USA Inc. | 60290-042 |
| Atorvastatin calcium | Atorvastatin 40 mg/1 | TabletOral | Umedica Laboratories USA Inc. | 60290-041 |