NDC codes

FDA NDC Directory
Product NDC (as listed)76282-672Labeler and product segments. Claims need a package NDC.
Product NDC at billing width76282-0672Add 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 NDC11-digit (billing)PackageCopy
76282-672-017628206720176282067201100 CAPSULE in 1 BOTTLE (76282-672-01)Marketed from Jan 28, 2020
76282-672-057628206720576282067205500 CAPSULE in 1 BOTTLE (76282-672-05)Marketed from Oct 28, 2021

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)
Ramipril
Generic name (nonproprietary)
ramipril
Active ingredients
Ramipril — 5 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Exelan Pharmaceuticals, Inc.NDC labeler code 76282
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077900
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers
Product ID 76282-672_37481fc5-771f-4dc7-aa06-6913ab75d485SPL ID 37481fc5-771f-4dc7-aa06-6913ab75d485SPL set ID 1e1dfacf-b831-4743-a874-9a5e5ef8a120RxCUI 198188, 198189, 261962, 845488UNII L35JN3I7SJUPC 0376282670010, 0376282672014, 0376282673011

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

N476282067201 followed by a unit qualifier and the quantity

Package 76282-0672-01. 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)

Ramipril is an angiotensin converting enzyme (ACE) inhibitor 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. It may be used alone or in combination with thiazide diuretics ( 1.1 ). In patients 55 years or older at high risk of developing a major cardiovascular event, ramipril is indicated to reduce the risk of myocardial infarction, stroke, or death from cardiovascular causes ( 1.2 ). Ramipril is indicated in stable patients who have demonstrated clinical signs of congestive heart failure post-myocardial infarction ( 1.3 ). 1.1 Hypertension…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 76282-672

What is NDC 76282-672?
76282-672 is the product NDC for Ramipril, Ramipril 5 mg/1 capsule, listed with the FDA by Exelan Pharmaceuticals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ramipril.
What is the active ingredient?
Ramipril.
Who is the labeler?
Exelan Pharmaceuticals, Inc., NDC labeler code 76282. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ramipril?
68 other product NDCs are listed under this name. See all Ramipril 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 Ramipril NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
RamiprilRamipril 2.5 mg/1CapsuleOralREMEDYREPACK INC.70518-460470518-4604-00
RamiprilRamipril 5 mg/1CapsuleOralREMEDYREPACK INC.70518-460770518-4607-00
RamiprilRamipril 2.5 mg/1CapsuleOralGSMS, Incorporated51407-70751407-0707-01
RamiprilRamipril 5 mg/1CapsuleOralGSMS, Incorporated51407-70851407-0708-01
RamiprilRamipril 10 mg/1CapsuleOralGSMS, Incorporated51407-70951407-0709-01
RamiprilRamipril 10 mg/1CapsuleOralNorthwind Health Company, LLC51655-90451655-0904-2651655-0904-52
RamiprilRamipril 2.5 mg/1CapsuleOralNorthwind Health Company, LLC51655-97551655-0975-52
RamiprilRamipril 5 mg/1CapsuleOralNorthwind Health Company, LLC51655-29651655-0296-52
RamiprilRamipril 10 mg/1CapsuleOralNorthwind Health Company, LLC51655-40651655-0406-52
RamiprilRamipril 10 mg/1CapsuleOralREMEDYREPACK INC.70518-303870518-3038-00

All 69 Ramipril NDCs

Other NDCs under ANDA 077900

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

FDA NDC Directory listings under ANDA 077900
ProductStrengthForm · routeLabelerProduct NDC
RamiprilRamipril 1.25 mg/1CapsuleOralHikma Pharmaceuticals USA Inc.0054-0106
RamiprilRamipril 2.5 mg/1CapsuleOralHikma Pharmaceuticals USA Inc.0054-0107
RamiprilRamipril 5 mg/1CapsuleOralHikma Pharmaceuticals USA Inc.0054-0108
RamiprilRamipril 10 mg/1CapsuleOralHikma Pharmaceuticals USA Inc.0054-0109
RamiprilRamipril 1.25 mg/1CapsuleOralExelan Pharmaceuticals, Inc.76282-670
RamiprilRamipril 2.5 mg/1CapsuleOralExelan Pharmaceuticals, Inc.76282-671
RamiprilRamipril 10 mg/1CapsuleOralExelan Pharmaceuticals, Inc.76282-673

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