diltiazem hydrochloride NDC 68788-7870

Product information

Brand name (proprietary)

diltiazem hydrochloride

Generic name (nonproprietary)

diltiazem hydrochloride

Active ingredients

Diltiazem hydrochloride — 120 mg/1

Dosage form

Capsule, Extended release

Route

Oral

Labeler

Preferred Pharmaceuticals Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 208783

Marketing start

Feb 15, 2021

Listing expires

Dec 31, 2027

Other FDA classes

Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)

Identifiers

Product ID 68788-7870_63cf2250-c568-4b74-849c-c39d9159560aSPL ID 63cf2250-c568-4b74-849c-c39d9159560aSPL set ID 3d594530-885f-45c7-b8a5-fd7e503ff83fRxCUI 830861UNII OLH94387TE

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

N468788787001 followed by a unit qualifier and the quantity Copy

Package 68788-7870-01. 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

Other NDCs under ANDA 208783

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