49884-006 : Sodium Phenylbutyrate .94 g/g Oral Powder


NDC: 49884-006
Labeler: Par Pharmaceutical, Inc.
Product Type: Human Prescription Drug
Drug Name:  Sodium Phenylbutyrate
Dosage Form: Oral Powder
Application #: ANDA203918
Rev. Date: 


NDC Package Codes:

  • 49884-006-04: 1 BOTTLE IN 1 CARTON (49884‑006‑04) > 250 G IN 1 BOTTLE

Active Ingredients:

  • Sodium Phenylbutyrate

Dosage Strength:

  • .94 g/g

Pharmaceutical Classes:

  • Ammonium Ion Binding Activity [MoA]
  • Nitrogen Binding Agent [EPC]

Related Products:

Based on records with the same trade name.
  • 49884-170 Sodium Phenylbutyrate 500 mg Oral Tablet by Par Pharmaceutical, Inc.
  • 42794-086 Sodium Phenylbutyrate .94 g/g Oral Powder by Sigmapharm Laboratories, LLC
  • 46672-851 Sodium Phenylbutyrate 500 mg Oral Tablet by Mikart, Inc.
  • 68462-853 Sodium Phenylbutyrate 500 mg Oral Tablet by Glenmark Pharmaceuticals Inc., USA

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.