Prescription drug · ANDA

Diltiazem Hydrochloride NDC 60687-717

Diltiazem hydrochloride 30 mg/1 · Tablet, Film coated · Oral · American Health Packaging

NDC codes

FDA NDC Directory
Product NDC (as listed)60687-717Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0717Add 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
60687-717-0160687071701100 BLISTER PACK in 1 CARTON (60687-717-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-717-11)Marketed from Mar 27, 2023

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)
Diltiazem Hydrochloride
Generic name (nonproprietary)
diltiazem hydrochloride
Active ingredients
Diltiazem hydrochloride — 30 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
American Health PackagingNDC labeler code 60687
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074185
Marketing start
Listing expires
Other FDA classes
Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)
Identifiers
Product ID 60687-717_5c50a33c-5543-8c01-e063-6394a90a83f5SPL ID 5c50a33c-5543-8c01-e063-6394a90a83f5
Pharmacologic class
Calcium Channel 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

N460687071701 followed by a unit qualifier and the quantity

Package 60687-0717-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 60687-717

What is NDC 60687-717?
60687-717 is the product NDC for Diltiazem Hydrochloride, Diltiazem hydrochloride 30 mg/1 tablet, film coated, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Diltiazem Hydrochloride.
What is the active ingredient?
Diltiazem hydrochloride.
Who is the labeler?
American Health Packaging, NDC labeler code 60687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Diltiazem Hydrochloride?
220 other product NDCs are listed under this name. See all Diltiazem Hydrochloride 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 Diltiazem Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Diltiazem hydrochlorideDiltiazem hydrochloride 120 mg/1TabletOralViona Pharmaceuticals Inc72578-20272578-0202-0172578-0202-05
Diltiazem hydrochlorideDiltiazem hydrochloride 30 mg/1TabletOralViona Pharmaceuticals Inc72578-19972578-0199-0172578-0199-05
Diltiazem hydrochlorideDiltiazem hydrochloride 60 mg/1TabletOralViona Pharmaceuticals Inc72578-20072578-0200-0172578-0200-05
Diltiazem hydrochlorideDiltiazem hydrochloride 90 mg/1TabletOralViona Pharmaceuticals Inc72578-20172578-0201-0172578-0201-05
Diltiazem hydrochlorideDiltiazem hydrochloride 60 mg/1TabletOralZydus Lifesciences Limited70771-193070771-1930-0170771-1930-05
Diltiazem hydrochlorideDiltiazem hydrochloride 30 mg/1TabletOralZydus Lifesciences Limited70771-192970771-1929-0170771-1929-05
Diltiazem hydrochlorideDiltiazem hydrochloride 90 mg/1TabletOralZydus Lifesciences Limited70771-193170771-1931-0170771-1931-05
Diltiazem hydrochlorideDiltiazem hydrochloride 120 mg/1TabletOralZydus Lifesciences Limited70771-193270771-1932-0170771-1932-05
Diltiazem HydrochlorideDiltiazem hydrochloride 120 mg/1Capsule, Extended releaseOralSafecor Health LLC48433-03248433-0032-20
Diltiazem HydrochlorideDiltiazem hydrochloride 60 mg/1Capsule, Extended releaseOralSafecor Health LLC48433-03048433-0030-20

All 221 Diltiazem Hydrochloride NDCs

Other NDCs under ANDA 074185

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

FDA NDC Directory listings under ANDA 074185
ProductStrengthForm · routeLabelerProduct NDC
Diltiazem HydrochlorideDiltiazem hydrochloride 120 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-0321
Diltiazem HydrochlorideDiltiazem hydrochloride 60 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8033
Diltiazem HydrochlorideDiltiazem hydrochloride 120 mg/1Tablet, Film coatedOralProficient Rx LP63187-769
Diltiazem HydrochlorideDiltiazem hydrochloride 60 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-728
Diltiazem HydrochlorideDiltiazem hydrochloride 60 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-0451
Diltiazem HydrochlorideDiltiazem hydrochloride 30 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-3659
Diltiazem HydrochlorideDiltiazem hydrochloride 60 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-020
Diltiazem HydrochlorideDiltiazem hydrochloride 30 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-0318
Diltiazem HydrochlorideDiltiazem hydrochloride 60 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-0319
Diltiazem HydrochlorideDiltiazem hydrochloride 90 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-0320
Diltiazem HydrochlorideDiltiazem hydrochloride 30 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8032

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Diltiazem Hydrochloride NDC 60687-717 | National Drug Code | Med-Code