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NDC 29300-0296-01 Ranolazine 500 mg/1 Details

Ranolazine 500 mg/1

Ranolazine is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Unichem Pharmaceuticals (USA), Inc.. The primary component is RANOLAZINE.

MedlinePlus Drug Summary

Ranolazine is used alone or with other medications to treat chronic angina (ongoing chest pain or pressure that is felt when the heart does not get enough oxygen). Ranolazine is in a class of medications called anti-anginals. The exact way that ranolazine works is not known at this time.

Related Packages: 29300-0296-01
Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Ranolazine

Product Information

NDC	29300-0296
Product ID	29300-296_429d55c7-1e90-4345-a6d4-59f689557f40
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Ranolazine
Proprietary Name Suffix	n/a
Non-Proprietary Name	Ranolazine
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	500
Active Ingredient Units	mg/1
Substance Name	RANOLAZINE
Labeler Name	Unichem Pharmaceuticals (USA), Inc.
Pharmaceutical Class	Anti-anginal [EPC], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA213083
Listing Certified Through	2024-12-31

Package

NDC 29300-0296-01 (29300029601)

Pricing Information	N/A
NDC Package Code	29300-296-01
Billing NDC	29300029601
Package	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (29300-296-01)
Marketing Start Date	2023-07-15
NDC Exclude Flag	N