What is NDC 70756-312?

70756-312 is the product NDC for Telmisartan, Telmisartan 20 mg/1 tablet, listed with the FDA by Lifestar Pharma LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Lifestar Pharma LLC, NDC labeler code 70756. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Telmisartan NDC 70756-312 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70756-312Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70756-0312Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
70756-312-30	70756031230	30 TABLET in 1 BOTTLE (70756-312-30)Marketed from Oct 15, 2024
70756-312-99	70756031299	10 BLISTER PACK in 1 CARTON (70756-312-99) / 10 TABLET in 1 BLISTER PACK (70756-312-01)Marketed from Oct 15, 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): Telmisartan
Generic name (nonproprietary): telmisartan
Active ingredients: Telmisartan — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Lifestar Pharma LLCNDC labeler code 70756
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218157
Marketing start: Oct 15, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 70756-312_28abd7a9-b660-4c91-b5f4-b65aa673fdbcSPL ID 28abd7a9-b660-4c91-b5f4-b65aa673fdbcSPL set ID 3ff464e6-7a36-4544-a06f-7848414f77fcRxCUI 205304, 205305, 282755UNII U5SYW473RQUPC 0370756313304, 0370756314301
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

N470756031230 followed by a unit qualifier and the quantity

Package 70756-0312-30. 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 Oct 18, 2024. 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 of phar…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70756-312

What is NDC 70756-312?: 70756-312 is the product NDC for Telmisartan, Telmisartan 20 mg/1 tablet, listed with the FDA by Lifestar Pharma LLC. It has 2 package NDCs, 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?: Lifestar Pharma LLC, NDC labeler code 70756. 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.

Other finished products listed under the same name: strengths, forms and labelers.

Other Telmisartan NDCs
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 40 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4034	68788-4034-03
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 40 mg/1	TabletOral	Lifestar Pharma LLC	70756-313	70756-0313-3070756-0313-80
Telmisartan	Telmisartan 80 mg/1	TabletOral	Lifestar Pharma LLC	70756-314	70756-0314-3070756-0314-80

All 80 Telmisartan NDCs

Other NDCs under ANDA 218157

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 218157
Product	Strength	Form · route	Labeler	Product NDC
Telmisartan	Telmisartan 40 mg/1	TabletOral	Lifestar Pharma LLC	70756-313
Telmisartan	Telmisartan 80 mg/1	TabletOral	Lifestar Pharma LLC	70756-314