0069-2650 : Procardia XL 30 mg 24 Hr Extended Release Tablet


NDC0069-2650
Labeler: Pfizer Laboratories Div Pfizer Inc
Product Type: Human Prescription Drug
Drug Name:  Procardia XL
Dosage Form: Oral Tablet, Film Coated, Extended Release
Application #: NDA019684
Rev. Date: 


Appearance:


Markings: PROCARDIA;XL;30
Shapes:  Round
Colors:  Pink
Size (mm): 9
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:

  • 0069-2650-41: 100 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BLISTER PACK (0069‑2650‑41)
  • 0069-2650-66: 100 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (0069‑2650‑66)
  • 0069-2650-72: 300 TABLET, FILM COATED, EXTENDED RELEASE IN 1 BOTTLE (0069‑2650‑72)

Active Ingredients:

  • Nifedipine

Dosage Strength:

  • 30 mg

Inactive Ingredients:

  • Cellulose Acetate
  • Hydroxypropyl Cellulose
  • Hypromelloses
  • Magnesium Stearate
  • Polyethylene Glycols
  • Ferric Oxide Red
  • Sodium Chloride
  • Titanium Dioxide

Pharmaceutical Classes:

  • Calcium Channel Antagonists [MoA]
  • Dihydropyridine Calcium Channel Blocker [EPC]
  • Dihydropyridines [CS]

Related Products:

Based on records with the same trade name.
  • 0069-2660 24 Hr Procardia XL 60 mg Extended Release Tablet by Pfizer Laboratories Div Pfizer Inc
  • 0069-2670 Procardia XL 90 mg 24 Hr Extended Release Tablet by Pfizer Laboratories Div Pfizer Inc
  • 70518-0600 Procardia 30 mg Oral Tablet, Film Coated, Extended Release by Remedyrepack Inc.

NDC QR Code

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NDC 0069-2650 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.