NDC 55670-805

moorebrand Ibuprofen

I Buprofen 200 Mg

moorebrand Ibuprofen is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Moore Medical Llc. The primary component is Ibuprofen.

• Product ID: 55670-805_7a8bfb67-ef65-0e5f-e053-2a91aa0ae864
• NDC: 55670-805
• Product Type: Human Otc Drug
• Proprietary Name: moorebrand Ibuprofen
• Generic Name: I Buprofen 200 Mg
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2016-02-01
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075010
• Labeler Name: Moore Medical LLC
• Substance Name: IBUPROFEN
• Active Ingredient Strength: 200 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 55670-805-04

200 PACKET in 1 BOX (55670-805-04) > 2 TABLET, FILM COATED in 1 PACKET (55670-805-99)

• Marketing Start Date: 2016-02-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55670-805-99 [55670080599]

moorebrand Ibuprofen TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075010
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-02-01

NDC 55670-805-04 [55670080504]

moorebrand Ibuprofen TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA075010
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-02-01

Drug Details

Active Ingredients

Ingredient	Strength
IBUPROFEN	200 mg/1

OpenFDA Data

• SPL SET ID: 2b84257d-d8a8-56fe-e054-00144ff88e88
• Manufacturer:
  • Moore Medical LLC
• UNII:
  • WK2XYI10QM
• RxNorm Concept Unique ID - RxCUI:
  • 310965
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
• NUI Code:
  • N0000000160
  • N0000175722
  • N0000175721