Prescription drug · ANDA
Clopidogrel NDC 68071-4138
Clopidogrel bisulfate 75 mg/1 · Tablet, Film coated · Oral · NuCare Pharmaceuticals,Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68071-4138-3 | 6807141380368071413803 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4138-3)Marketed from Oct 31, 2017 |
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)
- Clopidogrel
- Generic name (nonproprietary)
- clopidogrel
- Active ingredients
- Clopidogrel bisulfate — 75 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- NuCare Pharmaceuticals,Inc.NDC labeler code 68071
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 076999
- Marketing start
- Listing expires
- Other FDA classes
- Cytochrome P450 2C8 Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)P2Y12 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 68071-4138_2d3fdef2-fc4a-c8e1-e063-6394a90a0aa5SPL ID 2d3fdef2-fc4a-c8e1-e063-6394a90a0aa5SPL set ID 5cdca9bd-7042-142a-e053-2991aa0a9ca6RxCUI 309362UNII 08I79HTP27
- Pharmacologic class
- P2Y12 Platelet 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
N468071413803followed by a unit qualifier and the quantityPackage 68071-4138-03. 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
Current FDA label (SPL), effective . This label includes a boxed warning.
Indications (excerpt from the label)
Clopidogrel tablets are a P2Y 12 platelet inhibitor indicated for: Acute coronary syndrome For patients with non-ST-segment elevation ACS [unstable angina (UA)/non-ST-elevation myocardial infarction (NSTEMI)], clopidogrel tablets have been shown to reduce the rate of myocardial infarction (MI) and stroke. ( 1.1 ) For patients with ST-elevation myocardial infarction (STEMI), clopidogrel tablets have been shown to reduce the rate of MI and stroke. ( 1.1 ) Recent MI, recent stroke, or established peripheral arterial disease. Clopidogrel tablets have been shown to reduce the rate of MI and stroke. ( 1.2 ) 1.1 Acute Coronary Syndrome (ACS) Clopidogrel tablets are indicated to reduce the rate of m…
Excerpt only. Read the full label for complete information.
About NDC 68071-4138
- What is NDC 68071-4138?
- 68071-4138 is the product NDC for Clopidogrel, Clopidogrel bisulfate 75 mg/1 tablet, film coated, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Clopidogrel.
- What is the active ingredient?
- Clopidogrel bisulfate.
- Who is the labeler?
- NuCare Pharmaceuticals,Inc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Clopidogrel?
- 41 other product NDCs are listed under this name. See all Clopidogrel NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Clopidogrel products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Clopidogrelclopidogrel bisulfate | Clopidogrel bisulfate 75 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-4173 | 68788-4173-0368788-4173-0668788-4173-09 |
| Clopidogrelclopidogrel bisulfate | Clopidogrel bisulfate 75 mg/1 | Tablet, Film coatedOral | Cardinal Health 107, LLC | 55154-2149 | 55154-2149-00 |
| Clopidogrelclopidogrel bisulfate | Clopidogrel bisulfate 75 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4373 | 70518-4373-00 |
| Clopidogrelclopidogrel bisulfate | Clopidogrel bisulfate 75 mg/1 | Tablet, Film coatedOral | Novadoz Pharmaceuticals LLC | 72205-199 | 72205-0199-0172205-0199-0572205-0199-06+2 more |
| Clopidogrelclopidogrel bisulfate | Clopidogrel bisulfate 75 mg/1 | TabletOral | A-S Medication Solutions | 50090-7466 | 50090-7466-0050090-7466-01 |
| Clopidogrelclopidogrel bisulfate | Clopidogrel bisulfate 75 mg/1 | TabletOral | A-S Medication Solutions | 50090-7467 | 50090-7467-00 |
| Clopidogrelclopidogrel bisulfate | Clopidogrel bisulfate 75 mg/1 | TabletOral | Ascend Laboratories, LLC | 67877-276 | 67877-0276-0567877-0276-3067877-0276-90 |
| Clopidogrel | Clopidogrel 75 mg/1 | TabletOral | Camber Pharmaceuticals, Inc. | 31722-758 | 31722-0758-0531722-0758-3031722-0758-90 |
| Clopidogrel | Clopidogrel 300 mg/1 | TabletOral | Camber Pharmaceuticals, Inc. | 31722-759 | 31722-0759-0531722-0759-30 |
| Clopidogrelclopidogrel bisulfate | Clopidogrel bisulfate 75 mg/1 | Tablet, Film coatedOral | Westminster Pharmaceuticals, LLC | 69367-200 | 69367-0200-05 |
Other NDCs under ANDA 076999
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 |
|---|---|---|---|---|
| Clopidogrel | Clopidogrel bisulfate 75 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-7314 |
| Clopidogrel | Clopidogrel bisulfate 75 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 63187-362 |