United States · FDA National Drug Code directory
Procardia XL
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0069-2650_c24a0478-46d4-413a-8d48-c21af0bc10e4
- Product NDC
- 0069-2650
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- nifedipine
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Marketing category
- NDA
- Marketing start / end (source format)
- 19890906
- Source listing expiry
- 20261231
Source-listed ingredients
- NIFEDIPINE — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0069-2650-41) · 0069-2650-41
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2650-66) · 0069-2650-66
- 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2650-72) · 0069-2650-72
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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