NDC 70332-101

KETOPHENE

Ketophene

KETOPHENE is a Kit in the Human Prescription Drug category. It is labeled and distributed by California Pharmaceuticals, Llc. The primary component is .

• Product ID: 70332-101_c107b5b2-6eba-429b-a8de-d713b791d3fe
• NDC: 70332-101
• Product Type: Human Prescription Drug
• Proprietary Name: KETOPHENE
• Generic Name: Ketophene
• Dosage Form: Kit
• Marketing Start Date: 2016-01-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: California Pharmaceuticals, LLC
• Active Ingredient Strength: 0
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 70332-101-01

1 KIT in 1 KIT (70332-101-01) * 33.5 g in 1 BOTTLE * 100 g in 1 JAR * 33.5 g in 1 BOTTLE

• Marketing Start Date: 2016-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70332-101-01 [70332010101]

KETOPHENE KIT

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2016-01-01
• Inactivation Date: 2020-01-31

Drug Details

OpenFDA Data

• SPL SET ID: 271e6176-698a-30dd-e054-00144ff88e88
• Manufacturer:
  • California Pharmaceuticals, LLC