49349-494 : Asacol 400 mg Delayed Release Tablet


NDC49349-494
Labeler: Remedyrepack Inc.
Product Type: Human Prescription Drug
Drug Name:  Asacol
Dosage Form: Oral Tablet
Application #: NDA019651
Rev. Date: 


Appearance:


Markings: Asacol;NE
Shapes:  Oval
Colors:  Brown
Size (mm): 1
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 49349-494-02: 30 TABLET IN 1 BLISTER PACK (49349‑494‑02)
  • 49349-494-23: 180 TABLET IN 1 CANISTER (49349‑494‑23)

Active Ingredients:

  • Mesalamine

Dosage Strength:

  • 400 mg

Inactive Ingredients:

  • Ferric Oxide Red
  • Ferric Oxide Yellow
  • Lactose Monohydrate
  • Magnesium Stearate
  • Methacrylic Acid - Methyl Methacrylate Copolymer (1:2)
  • Polyethylene Glycol
  • Povidone
  • Sodium Starch Glycolate Type a Potato
  • Talc

Pharmaceutical Classes:

  • Aminosalicylate [EPC]
  • Aminosalicylic Acids [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
  • 49349-678 Mesalamine 400 mg Delayed Release Tablet by Remedyrepack Inc.
  • 49349-951 Mesalamine 400 mg Delayed Release Tablet by Remedyrepack Inc.
  • 0023-0752 Asacol 400 mg Oral Tablet, Delayed Release by Allergan, Inc.
  • 0179-0111 Asacol 400 mg Delayed Release Tablet by Kaiser Foundation Hospitals
  • 0430-0752 Asacol 400 mg/1 Oral Tablet, Delayed Release by Warner Chilcott (Us), LLC
  • 49999-969 Asacol 400 mg Delayed Release Tablet by Lake Erie Medical & Surgical Supply Dba Quality Care Products LLC
  • 53808-0205 Asacol 400 mg Delayed Release Tablet by State of Florida Doh Central Pharmacy
  • 53808-0823 Asacol 400 mg Oral Tablet, Delayed Release by State of Florida Doh Central Pharmacy
  • 55154-2305 Asacol 400 mg Delayed Release Tablet by Cardinal Health
  • 55154-8607 Asacol 400 mg Delayed Release Tablet by Cardinal Health
  • 68084-568 Asacol 400 mg Delayed Release Tablet by American Health Packaging

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.