NDC 70518-2006

SUPRAX

Cefixime

SUPRAX is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Cefixime.

• Product ID: 70518-2006_86244478-07f0-94cf-e053-2a91aa0ac94a
• NDC: 70518-2006
• Product Type: Human Prescription Drug
• Proprietary Name: SUPRAX
• Generic Name: Cefixime
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 2019-04-09
• Marketing Category: NDA / NDA
• Application Number: NDA203195
• Labeler Name: REMEDYREPACK INC.
• Substance Name: CEFIXIME
• Active Ingredient Strength: 400 mg/1
• Pharm Classes: Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 70518-2006-0

1 CAPSULE in 1 BOTTLE, PLASTIC (70518-2006-0)

• Marketing Start Date: 2019-04-09
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70518-2006-0 [70518200600]

SUPRAX CAPSULE

• Marketing Category: NDA
• Application Number: NDA203195
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-04-09

Drug Details

Active Ingredients

Ingredient	Strength
CEFIXIME	400 mg/1

OpenFDA Data

• SPL SET ID: a222969e-9ebf-44cb-98b5-521d45c72c7a
• Manufacturer:
  • REMEDYREPACK INC.
• UNII:
  • 97I1C92E55

Pharmacological Class

• Cephalosporin Antibacterial [EPC]
• Cephalosporins [CS]
• 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