Prescription drug · ANDA
Telmisartan NDC 68788-4034
Telmisartan 40 mg/1 · Tablet · Oral · Preferred Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68788-4034-3 | 6878840340368788403403 | 30 TABLET in 1 BOTTLE (68788-4034-3)Marketed from Sep 29, 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)
- Telmisartan
- Generic name (nonproprietary)
- telmisartan
- Active ingredients
- Telmisartan — 40 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Preferred Pharmaceuticals Inc.NDC labeler code 68788
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090032
- Marketing start
- Listing expires
- Other FDA classes
- Angiotensin 2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 68788-4034_bf8e95fa-d181-4b46-8609-497e14a73dc1SPL ID bf8e95fa-d181-4b46-8609-497e14a73dc1SPL set ID bf8e95fa-d181-4b46-8609-497e14a73dc1RxCUI 205304UNII U5SYW473RQ
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
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
N468788403403followed by a unit qualifier and the quantityPackage 68788-4034-03. 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)
Telmisartan tablets are an angiotensin II receptor blocker (ARB) indicated for: • Treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) • Cardiovascular (CV) risk reduction in patients unable to take ACE inhibitors ( 1.2 ) 1.1 Hypertension Telmisartan tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety…
Excerpt only. Read the full label for complete information.
About NDC 68788-4034
- What is NDC 68788-4034?
- 68788-4034 is the product NDC for Telmisartan, Telmisartan 40 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Telmisartan.
- What is the active ingredient?
- Telmisartan.
- Who is the labeler?
- Preferred Pharmaceuticals Inc., NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Telmisartan?
- 79 other product NDCs are listed under this name. See all Telmisartan NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Telmisartan products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Telmisartan | Telmisartan 20 mg/1 | TabletOral | Redpharm Drug | 67296-2284 | 67296-2284-09 |
| Telmisartan | Telmisartan 40 mg/1 | TabletOral | NorthStar RxLLC | 72603-832 | 72603-0832-01 |
| Telmisartan | Telmisartan 20 mg/1 | TabletOral | NorthStar RxLLC | 72603-831 | 72603-0831-01 |
| Telmisartan | Telmisartan 80 mg/1 | TabletOral | NorthStar RxLLC | 72603-833 | 72603-0833-01 |
| Telmisartan | Telmisartan 20 mg/1 | TabletOral | Macleods Pharmaceuticals Limited | 33342-118 | 33342-0118-0733342-0118-10 |
| Telmisartan | Telmisartan 40 mg/1 | TabletOral | Macleods Pharmaceuticals Limited | 33342-119 | 33342-0119-0733342-0119-10 |
| Telmisartan | Telmisartan 80 mg/1 | TabletOral | Macleods Pharmaceuticals Limited | 33342-120 | 33342-0120-0733342-0120-10 |
| Telmisartan | Telmisartan 80 mg/1 | TabletOral | Lifestar Pharma LLC | 70756-314 | 70756-0314-3070756-0314-80 |
| Telmisartan | Telmisartan 20 mg/1 | TabletOral | Lifestar Pharma LLC | 70756-312 | 70756-0312-3070756-0312-99 |
| Telmisartan | Telmisartan 40 mg/1 | TabletOral | Lifestar Pharma LLC | 70756-313 | 70756-0313-3070756-0313-80 |
Other NDCs under ANDA 090032
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 |
|---|---|---|---|---|
| Telmisartan | Telmisartan 80 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-5178 |
| Telmisartan | Telmisartan 20 mg/1 | TabletOral | Glenmark Pharmaceuticals Inc., USA | 68462-199 |
| Telmisartan | Telmisartan 40 mg/1 | TabletOral | Glenmark Pharmaceuticals Inc., USA | 68462-200 |
| Telmisartan | Telmisartan 80 mg/1 | TabletOral | Glenmark Pharmaceuticals Inc., USA | 68462-201 |
| Telmisartan | Telmisartan 80 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-2572 |
| Telmisartan | Telmisartan 80 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1723 |