0071-0532 : Accupril 20 mg Oral Tablet


NDC0071-0532
Labeler: Parke-davis Div of Pfizer Inc
Product Type: Human Prescription Drug
Drug Name:  Accupril
Dosage Form: Oral Tablet, Film Coated
Application #: NDA019885
Rev. Date: 


Appearance:


Markings: PD;532;20
Shapes:  Round
Colors:  Brown
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.

PD 532 20: (0071-0532) Accupril 20 mg Oral Tablet by Parke-davis Div of Pfizer 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:

  • 0071-0532-23: 90 TABLET, FILM COATED IN 1 BOTTLE (0071‑0532‑23)
  • 0071-0532-40: 100 BLISTER PACK IN 1 CARTON (0071‑0532‑40) > 1 TABLET, FILM COATED IN 1 BLISTER PACK

Active Ingredients:

  • Quinapril Hydrochloride

Dosage Strength:

  • 20 mg

Inactive Ingredients:

  • Candelilla Wax
  • Crospovidone
  • Gelatin
  • Lactose
  • Magnesium Carbonate
  • Magnesium Stearate
  • Ferric Oxide Red
  • Titanium Dioxide

Pharmaceutical Classes:

  • Angiotensin Converting Enzyme Inhibitor [EPC]
  • Angiotensin-converting Enzyme Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 0071-0527 Accupril 5 mg Oral Tablet by Parke-davis Div of Pfizer Inc
  • 0071-0530 Accupril 10 mg Oral Tablet by Parke-davis Div of Pfizer Inc
  • 0071-0535 Accupril 40 mg Oral Tablet by Parke-davis Div of Pfizer Inc
  • 0071-1205 Quinapril Hydrochloride by Parke-davis Div of Pfizer Inc
  • 0071-1410 Quinapril Hydrochloride by Parke-davis Div of Pfizer Inc
  • 0071-1620 Quinapril Hydrochloride by Parke-davis Div of Pfizer Inc
  • 0071-1840 Quinapril Hydrochloride by Parke-davis Div of Pfizer Inc
  • 55154-2418 Accupril 10 mg Oral Tablet by Cardinal Health
  • 55154-2423 Accupril 20 mg Oral Tablet by Cardinal Health
  • 63629-1242 Accupril 40 mg Oral Tablet by Bryant Ranch Prepack

NDC QR Code

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NDC 0071-0532 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.