41190-047 : Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet


NDC: 41190-047
Labeler: Wakefern Food Corporation
Product Type: Human OTC Drug
Drug Name:  Shoprite Acid Reducer
Dosage Form: Oral Tablet
Application #: ANDA078653
Rev. Date: 


Appearance:


Markings: W;741
Shapes:  Hexagon (6 sides)
Colors:  Orange
Size (mm): 10
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:

  • 41190-047-62: 3 BLISTER PACK IN 1 CARTON (41190‑047‑62) > 8 TABLET IN 1 BLISTER PACK
  • 41190-047-71: 1 BOTTLE IN 1 CARTON (41190‑047‑71) > 50 TABLET IN 1 BOTTLE

Active Ingredients:

  • Ranitidine Hydrochloride

Dosage Strength:

  • 150 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Croscarmellose Sodium
  • Diethyl Phthalate
  • Hypromelloses
  • Magnesium Stearate
  • Cellulose, Microcrystalline
  • Titanium Dioxide
  • Ferric Oxide Red

Related Products:

Based on records with the same trade name.
  • 41190-141 Famotidine 10 mg Oral Tablet by Wakefern Food Corporation
  • 41190-194 Famotidine 20 mg Oral Tablet by Wakefern Food Corporation
  • 41190-852 Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet by Wakefern Food Corporation
  • 41190-950 Ranitidine 150 mg (As Ranitidine Hydrochloride 168 mg) Oral Tablet by Wakefern Food Corporation

NDC QR Code

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

NDC 41190-047 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.