49483-003 : Bisacodyl 5 mg Delayed Release Tablet


NDC: 49483-003
Labeler: Time Cap Laboratories, Inc
Product Type: Human OTC Drug
Drug Name:  Stimulant Laxative
Dosage Form: Oral Tablet, Delayed Release
Application #: part334
Rev. Date: 


Appearance:


Markings: TCL003
Shapes:  Round
Colors:  Orange
Size (mm): 5
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:

  • 49483-003-00: 100000 TABLET, DELAYED RELEASE IN 1 CARTON (49483‑003‑00)
  • 49483-003-01: 100 TABLET, DELAYED RELEASE IN 1 BOTTLE, PLASTIC (49483‑003‑01)
  • 49483-003-10: 1000 TABLET, DELAYED RELEASE IN 1 BOTTLE, PLASTIC (49483‑003‑10)
  • 49483-003-52: 25 TABLET, DELAYED RELEASE IN 1 BLISTER PACK (49483‑003‑52)

Active Ingredients:

  • Bisacodyl

Dosage Strength:

  • 5 mg

Inactive Ingredients:

  • Acacia
  • Calcium Sulfate Anhydrous
  • Anhydrous Lactose
  • Carnauba Wax
  • Silicon Dioxide
  • Starch, Corn
  • D&c Yellow No. 10
  • Fd&c Yellow No. 6
  • Gelatin
  • Ferrosoferric Oxide
  • Ferric Oxide Yellow
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Polyethylene Glycol 400
  • Polyvinyl Acetate Phthalate
  • Povidone
  • Sodium Starch Glycolate Type a Corn
  • Stearic Acid
  • Sucrose
  • Talc
  • Titanium Dioxide

Pharmaceutical Classes:

  • Increased Large Intestinal Motility [PE]
  • Stimulant Laxative [EPC]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Related Products:

Based on records with the same trade name.
  • 61715-038 Bisacodyl 5 mg Delayed Release Tablet by Preferred Plus (Kinray)
  • 69842-747 Stimulant Laxative 15 mg Oral Tablet, Sugar Coated by Cvs Pharmacy
  • 70000-0228 Stimulant Laxative 5 mg Oral Tablet, Delayed Release by Cardinal Health
  • 72476-845 Stimulant Laxative 5 mg Oral Tablet, Delayed Release by Retail Business Services, LLC

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 49483-003 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.