Prescription drug · ANDA
Clopidogrel (Clopidogrel bisulfate) NDC 72205-199
Clopidogrel bisulfate 75 mg/1 · Tablet, Film coated · Oral · Novadoz Pharmaceuticals LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72205-199-01 | 7220501990172205019901 | 1000 TABLET, FILM COATED in 1 BOTTLE (72205-199-01)Marketed from Nov 12, 2025 | |
| 72205-199-05 | 7220501990572205019905 | 500 TABLET, FILM COATED in 1 BOTTLE (72205-199-05)Marketed from Nov 22, 2024 | |
| 72205-199-06 | 7220501990672205019906 | 10 BLISTER PACK in 1 CARTON (72205-199-06) / 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-199-11)Marketed from Nov 22, 2024 | |
| 72205-199-30 | 7220501993072205019930 | 30 TABLET, FILM COATED in 1 BOTTLE (72205-199-30)Marketed from Nov 22, 2024 | |
| 72205-199-90 | 7220501999072205019990 | 90 TABLET, FILM COATED in 1 BOTTLE (72205-199-90)Marketed from Nov 22, 2024 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 bisulfate
- Active ingredients
- Clopidogrel bisulfate — 75 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Novadoz Pharmaceuticals LLCNDC labeler code 72205
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 215388
- Marketing start
- Listing expires
- Other FDA classes
- Cytochrome P450 2C8 Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)P2Y12 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 72205-199_0b4edca9-12af-4534-baad-4fa5c1cc9ac8SPL ID 0b4edca9-12af-4534-baad-4fa5c1cc9ac8SPL set ID 1447a095-c663-4f05-91d4-f09bfc0c3d42RxCUI 309362UNII 08I79HTP27UPC 0372205199057, 0372205199309, 0372205199903, 0372205199019
- 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
N472205019901followed by a unit qualifier and the quantityPackage 72205-0199-01. 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 has been shown to reduce the rate of myocardial infarction (MI) and stroke. ( 1.1 ) – For patients with ST-elevation myocardial infarction (STEMI), clopidogrel tablets has been shown to reduce the rate of MI and stroke. ( 1.1 ) Recent MI, recent stroke, or established peripheral arterial disease. Clopidogrel tablets has 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 …
Excerpt only. Read the full label for complete information.
About NDC 72205-199
- What is NDC 72205-199?
- 72205-199 is the product NDC for Clopidogrel (clopidogrel bisulfate), Clopidogrel bisulfate 75 mg/1 tablet, film coated, listed with the FDA by Novadoz Pharmaceuticals LLC. It has 5 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Clopidogrel (Clopidogrel bisulfate).
- What is the active ingredient?
- Clopidogrel bisulfate.
- Who is the labeler?
- Novadoz Pharmaceuticals LLC, NDC labeler code 72205. 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 | 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 |
| Clopidogrel | Clopidogrel bisulfate 75 mg/1 | TabletOral | NorthStar RxLLC | 16714-052 | 16714-0052-0116714-0052-0216714-0052-03+3 more |
Other NDCs under ANDA 215388
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 |
|---|---|---|---|---|
| Clopidogrelclopidogrel bisulfate | Clopidogrel bisulfate 75 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-4173 |