Tiadylt ER (Diltiazem hydrochloride) NDC 70771-1040

Product information

Brand name (proprietary)

Tiadylt ER

Generic name (nonproprietary)

diltiazem hydrochloride

Active ingredients

Diltiazem hydrochloride — 420 mg/1

Dosage form

Capsule, Extended release

Route

Oral

Labeler

Zydus Lifesciences LimitedNDC labeler code 70771

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 206641

Marketing start

Nov 8, 2017

Listing expires

Dec 31, 2026

Other FDA classes

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

Identifiers

Product ID 70771-1040_302fc306-6fbe-4567-b5ce-dcc5a45ba894SPL ID 302fc306-6fbe-4567-b5ce-dcc5a45ba894SPL set ID d88e3546-3984-4dc9-893a-a29e95804550RxCUI 830795, 830801, 830837, 830845, 830861, 831359, 1988308, 1988311, 1988316, 1988319, 1988324, 1988330UNII OLH94387TEUPC 0370771103997

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

N470771104000 followed by a unit qualifier and the quantity Copy

Package 70771-1040-00. 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

About NDC 70771-1040

What is NDC 70771-1040?

70771-1040 is the product NDC for Tiadylt ER (diltiazem hydrochloride), Diltiazem hydrochloride 420 mg/1 capsule, extended release, listed with the FDA by Zydus Lifesciences Limited. It has 5 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Tiadylt ER (Diltiazem hydrochloride).

What is the active ingredient?

Diltiazem hydrochloride.

Who is the labeler?

Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Tiadylt ER?

12 other product NDCs are listed under this name. See all Tiadylt ER NDCs.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory. See Billing references above.

Related NDCs: other Tiadylt ER products

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

All 13 Tiadylt ER NDCs

Other NDCs under ANDA 206641

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