NDC 37808-200

childrens ibuprofen

Ibuprofen

childrens ibuprofen is a Oral Suspension in the Human Otc Drug category. It is labeled and distributed by H E B. The primary component is Ibuprofen.

• Product ID: 37808-200_7c800d9e-1a80-494b-80b7-e4cdb6472849
• NDC: 37808-200
• Product Type: Human Otc Drug
• Proprietary Name: childrens ibuprofen
• Generic Name: Ibuprofen
• Dosage Form: Suspension
• Route of Administration: ORAL
• Marketing Start Date: 2002-06-19
• Marketing Category: ANDA / ANDA
• Application Number: ANDA074937
• Labeler Name: H E B
• Substance Name: IBUPROFEN
• Active Ingredient Strength: 100 mg/5mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 37808-200-26

1 BOTTLE in 1 CARTON (37808-200-26) > 120 mL in 1 BOTTLE

• Marketing Start Date: 2002-06-19
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 37808-200-26 [37808020026]

childrens ibuprofen SUSPENSION

• Marketing Category: ANDA
• Application Number: ANDA074937
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2002-06-19

Drug Details

Active Ingredients

Ingredient	Strength
IBUPROFEN	100 mg/5mL

OpenFDA Data

• SPL SET ID: e7e2b766-6d05-49e2-9e88-72454b857935
• Manufacturer:
  • H E B
• UNII:
  • WK2XYI10QM
• RxNorm Concept Unique ID - RxCUI:
  • 197803
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
• NUI Code:
  • N0000000160
  • N0000175722
  • N0000175721