NDC 27437-203

SUPRAX

Cefixime

SUPRAX is a Oral Tablet, Chewable in the Human Prescription Drug category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is Cefixime.

• Product ID: 27437-203_0e44b51b-cba9-4dc5-8ee1-2d151ad24def
• NDC: 27437-203
• Product Type: Human Prescription Drug
• Proprietary Name: SUPRAX
• Generic Name: Cefixime
• Dosage Form: Tablet, Chewable
• Route of Administration: ORAL
• Marketing Start Date: 2012-12-05
• Marketing Category: ANDA / ANDA
• Application Number: ANDA065380
• Labeler Name: Lupin Pharmaceuticals, Inc.
• Substance Name: CEFIXIME
• Active Ingredient Strength: 100 mg/1
• Pharm Classes: Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 27437-203-02

1 BLISTER PACK in 1 CARTON (27437-203-02) > 1 TABLET, CHEWABLE in 1 BLISTER PACK

• Marketing Start Date: 2012-12-05
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 27437-203-08 [27437020308]

SUPRAX TABLET, CHEWABLE

• Marketing Category: ANDA
• Application Number: ANDA065380
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-10-11

NDC 27437-203-10 [27437020310]

SUPRAX TABLET, CHEWABLE

• Marketing Category: ANDA
• Application Number: ANDA065380
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-10-11

NDC 27437-203-02 [27437020302]

SUPRAX TABLET, CHEWABLE

• Marketing Category: ANDA
• Application Number: ANDA065380
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-12-05

NDC 27437-203-11 [27437020311]

SUPRAX TABLET, CHEWABLE

• Marketing Category: ANDA
• Application Number: ANDA065380
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2012-10-11

NDC 27437-203-13 [27437020313]

SUPRAX TABLET, CHEWABLE

• Marketing Category: ANDA
• Application Number: ANDA065380
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2012-10-11
• Marketing End Date: 2013-06-21

Drug Details

Active Ingredients

Ingredient	Strength
CEFIXIME	100 mg/1

OpenFDA Data

• SPL SET ID: d0fd45bd-7d52-4fa6-a5f7-f46d5651ffa2
• Manufacturer:
  • Lupin Pharmaceuticals, Inc.
• UNII:
  • 97I1C92E55
• RxNorm Concept Unique ID - RxCUI:
  • 1043025
  • 1043030
  • 1043031
  • 1373016
  • 1373014
  • 1043022
  • 213927
  • 419849
  • 705008
  • 409823
  • 1372999
  • 197451
• UPC Code:
  • 0327437206059

Pharmacological Class

• Cephalosporin Antibacterial [EPC]
• Cephalosporins [CS]

NDC Crossover Matching brand name "SUPRAX" or generic name "Cefixime"

NDC	Brand Name	Generic Name
27437-201	SUPRAX	cefixime
27437-203	SUPRAX	cefixime
27437-205	SUPRAX	cefixime
27437-206	SUPRAX	cefixime
27437-207	SUPRAX	cefixime
27437-208	SUPRAX	cefixime
43063-537	SUPRAX	cefixime
54348-797	SUPRAX	CEFIXIME
68180-202	SUPRAX	SUPRAX
70518-1020	SUPRAX	SUPRAX
70934-079	SUPRAX	SUPRAX
70518-2006	SUPRAX	SUPRAX
16714-766	Cefixime	cefixime
16714-767	Cefixime	cefixime
43598-673	Cefixime	Cefixime
43598-674	Cefixime	Cefixime
62250-663	Cefixime	cefixime
62250-664	Cefixime	cefixime