70786-0900 : Glipizide ER 2.5 mg Oral Tablet, Film Coated, Extended Release


NDC: 70786-0900
Labeler: Unit Dose Services
Product Type: Human Prescription Drug
Drug Name:  Glipizide ER
Dosage Form: Oral Tablet, Film Coated, Extended Release
Application #: ANDA076467
Rev. Date: 


Appearance:


Markings: WPI;900
Shapes:  Round
Colors:  Orange
Size (mm): 6
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.

WPI 900: (0228-2898) Glipizide ER 2.5 mg Oral Tablet, Film Coated, Extended Release by Unit Dose Services
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.

NDC Package Codes:

  • 70786-0900-1: 30 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (70786‑0900‑1)

Active Ingredients:

  • Glipizide

Dosage Strength:

  • 2.5 mg

Inactive Ingredients:

  • Acetyltributyl Citrate
  • Hydroxyethyl Cellulose (2000 Mpa.s At 1%)
  • Hydroxypropyl Cellulose (Type H)
  • Lactose Monohydrate
  • Magnesium Stearate
  • Methacrylic Acid - Methyl Methacrylate Copolymer (1:1)
  • Polyethylene Glycols
  • Fd&c Yellow No. 6
  • Shellac
  • Isopropyl Alcohol
  • Ferrosoferric Oxide
  • Butyl Alcohol
  • Propylene Glycol
  • Ammonia

Pharmaceutical Classes:

  • Sulfonylurea [EPC]
  • Sulfonylurea Compounds [Chemical/Ingredient]

Related Products:

Based on records with the same trade name.
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  • 68071-4133 Glipizide ER 5 mg Oral Tablet, Film Coated, Extended Release by Nucare Pharmaceuticals, Inc.
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NDC QR Code

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NDC 70786-0900 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.