68788-6390 : Lansoprazole 15 mg Oral Capsule, Delayed Release


NDC: 68788-6390
Labeler: Preferred Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name:  Lansoprazole
Dosage Form: Oral Capsule, Delayed Release
Application #: ANDA091269
Rev. Date: 


Appearance:


Markings: RDY;398
Shapes:  Capsule
Colors:  Pink / Green
Size (mm): 16
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.

RDY 398: (55111-398) Lansoprazole 15 mg Oral Capsule, Delayed Release by Preferred Pharmaceuticals Inc.
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:

  • 68788-6390-1: 100 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (68788‑6390‑1)
  • 68788-6390-2: 20 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (68788‑6390‑2)
  • 68788-6390-3: 30 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (68788‑6390‑3)
  • 68788-6390-4: 14 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (68788‑6390‑4)
  • 68788-6390-6: 60 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (68788‑6390‑6)
  • 68788-6390-7: 40 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (68788‑6390‑7)
  • 68788-6390-8: 120 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (68788‑6390‑8)
  • 68788-6390-9: 90 CAPSULE, DELAYED RELEASE IN 1 BOTTLE (68788‑6390‑9)

Active Ingredients:

  • Lansoprazole

Dosage Strength:

  • 15 mg

Inactive Ingredients:

  • Ammonia
  • Hydroxypropyl Cellulose (1200000 Mw)
  • Low-substituted Hydroxypropyl Cellulose, Unspecified
  • Magnesium Carbonate
  • Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type a
  • Polyethylene Glycol, Unspecified
  • Polysorbate 80
  • Propylene Glycol
  • Shellac
  • Starch, Corn
  • Sucrose
  • Raw Sugar
  • Titanium Dioxide
  • Talc
  • Gelatin, Unspecified
  • Ferric Oxide Red
  • Ferric Oxide Yellow
  • Fd&c Blue No. 2
  • Sodium Lauryl Sulfate

Pharmaceutical Classes:

  • Proton Pump Inhibitor [EPC]
  • Proton Pump Inhibitors [MoA]
  • Inhibition Gastric Acid Secretion [PE]

Related Products:

Based on records with the same trade name.
  • 68788-6389 Lansoprazole 15 mg Oral Capsule, Delayed Release by Preferred Pharmaceuticals Inc.
  • 68788-7385 Lansoprazole 30 mg Oral Capsule, Delayed Release Pellets by Preferred Pharmaceuticals Inc.
  • 68788-7789 Lansoprazole 15 mg Oral Capsule, Delayed Release Pellets by Preferred Pharmaceuticals Inc.
  • 68788-8621 Lansoprazole 30 mg Oral Capsule, Delayed Release by Preferred Pharmaceuticals Inc.
  • 68788-8915 Lansoprazole 30 mg Oral Capsule, Delayed Release by Preferred Pharmaceuticals Inc.
  • 68788-7742 Lansoprazole 30 mg Oral Capsule, Delayed Release by Preferred Pharmaceuticals, Inc.
  • 68788-8999 Lansoprazole 15 mg Delayed Release Capsule by Preferred Pharmaceuticals, Inc.
  • 68788-9269 Lansoprazole 30 mg Oral Capsule, Delayed Release Pellets by Preferred Pharmaceuticals, Inc.
  • 68788-9281 Lansoprazole 30 mg Oral Capsule, Delayed Release by Preferred Pharmaceuticals, Inc.
  • 68788-9406 Lansoprazole 30 mg Oral Capsule, Delayed Release by Preferred Pharmaceuticals, Inc.
  • 68788-9677 Lansoprazole 15 mg Delayed Release Capsule by Preferred Pharmaceuticals, Inc.
  • 0093-3008 Lansoprazole 15 mg Oral Tablet, Orally Disintegrating, Delayed Release by Teva Pharmaceuticals USA, Inc.
  • 0093-3009 Lansoprazole 30 mg Oral Tablet, Orally Disintegrating, Delayed Release by Teva Pharmaceuticals USA, Inc.
  • 0093-7350 Lansoprazole 15 mg Delayed Release Capsule by Teva Pharmaceuticals USA Inc
  • 0093-7351 Lansoprazole 30 mg Delayed Release Capsule by Teva Pharmaceuticals USA Inc
  • 0363-0037 Lansoprazole 15 mg Oral Capsule, Delayed Release by Walgreens Company
  • 0363-0739 Lansoprazole 15 mg/1 Oral Capsule, Delayed Release by Walgreen Co
  • 0363-1212 Lansoprazole 15 mg Oral Capsule, Delayed Release by Walgreen Company
  • 0363-1419 Lansoprazole 15 mg Oral Tablet, Orally Disintegrating, Delayed Release by Walgreen Company
  • 0363-4069 Lansoprazole 15 mg Oral Capsule, Delayed Release by Walgreen Company
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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.