NDC 55111-329

Nateglinide

Nateglinide

Nateglinide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Dr. Reddy's Laboratories Limited. The primary component is Nateglinide.

• Product ID: 55111-329_1f405b49-b32b-876e-3ef0-ea4f8b9473c5
• NDC: 55111-329
• Product Type: Human Prescription Drug
• Proprietary Name: Nateglinide
• Generic Name: Nateglinide
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2009-09-09
• Marketing Category: ANDA / ANDA
• Application Number: ANDA077461
• Labeler Name: Dr. Reddy's Laboratories Limited
• Substance Name: NATEGLINIDE
• Active Ingredient Strength: 120 mg/1
• Pharm Classes: Glinide [EPC],Potassium Channel Antagonists [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 55111-329-01

100 TABLET in 1 BOTTLE (55111-329-01)

• Marketing Start Date: 2009-09-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55111-329-30 [55111032930]

Nateglinide TABLET

• Marketing Category: ANDA
• Application Number: ANDA077461
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-09-09

NDC 55111-329-90 [55111032990]

Nateglinide TABLET

• Marketing Category: ANDA
• Application Number: ANDA077461
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2009-09-09

NDC 55111-329-79 [55111032979]

Nateglinide TABLET

• Marketing Category: ANDA
• Application Number: ANDA077461
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-09-09

NDC 55111-329-05 [55111032905]

Nateglinide TABLET

• Marketing Category: ANDA
• Application Number: ANDA077461
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-09-09

NDC 55111-329-01 [55111032901]

Nateglinide TABLET

• Marketing Category: ANDA
• Application Number: ANDA077461
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-09-09

NDC 55111-329-78 [55111032978]

Nateglinide TABLET

• Marketing Category: ANDA
• Application Number: ANDA077461
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-09-09

Drug Details

Active Ingredients

Ingredient	Strength
NATEGLINIDE	120 mg/1

OpenFDA Data

• SPL SET ID: f7b28951-76d2-cabd-64a1-b74aa225c6e9
• Manufacturer:
  • Dr. Reddy's Laboratories Limited
• UNII:
  • 41X3PWK4O2
• RxNorm Concept Unique ID - RxCUI:
  • 311919
  • 314142
• UPC Code:
  • 0355111329909

Pharmacological Class

• Glinide [EPC]
• Potassium Channel Antagonists [MoA]
• Glinide [EPC]
• Potassium Channel Antagonists [MoA]

Medicade Reported Pricing

55111032990 NATEGLINIDE 120 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Nateglinide" or generic name "Nateglinide"

NDC	Brand Name	Generic Name
0591-3354	Nateglinide	Nateglinide
0591-3355	Nateglinide	Nateglinide
0615-7585	Nateglinide	Nateglinide
0615-7586	Nateglinide	Nateglinide
16571-758	NATEGLINIDE	NATEGLINIDE
16571-759	NATEGLINIDE	NATEGLINIDE
42291-636	Nateglinide	Nateglinide
42291-637	Nateglinide	Nateglinide
49884-984	Nateglinide	Nateglinide
49884-985	Nateglinide	Nateglinide
51407-656	Nateglinide	nateglinide
51407-657	Nateglinide	nateglinide
52536-063	Nateglinide	Nateglinide
52536-067	Nateglinide	Nateglinide
55111-328	Nateglinide	Nateglinide
55111-329	Nateglinide	Nateglinide
60429-434	Nateglinide	Nateglinide
60429-435	Nateglinide	Nateglinide
60687-673	Nateglinide	nateglinide
60687-684	Nateglinide	nateglinide
64380-167	Nateglinide	nateglinide
64380-168	Nateglinide	nateglinide
68084-458	Nateglinide	Nateglinide
68084-459	Nateglinide	Nateglinide
68382-721	Nateglinide	Nateglinide
68382-722	Nateglinide	Nateglinide
70771-1016	Nateglinide	Nateglinide
70771-1015	Nateglinide	Nateglinide
71209-030	Nateglinide	Nateglinide
71209-031	Nateglinide	Nateglinide
75834-205	NATEGLINIDE	NATEGLINIDE
75834-206	NATEGLINIDE	NATEGLINIDE
0078-0351	Starlix	nateglinide
0078-0352	Starlix	nateglinide