PROCARDIA XL — FDA application NDA019684
Listed sponsor: PFIZER · PFE company profile · exact_unique
Sponsor as listed in Drugs@FDA at retrieval (2026-08-07); FDA sponsor listings can lag ownership transfers.
FDA application facts
| Product | FDA-listed trade name | Active ingredient | Dosage form | Route | Strength | Marketing status | TE code | RLD |
|---|---|---|---|---|---|---|---|---|
| 001 | PROCARDIA XL | NIFEDIPINE | TABLET, EXTENDED RELEASE | ORAL | 30MG | Prescription | AB2 | Yes |
| 002 | PROCARDIA XL | NIFEDIPINE | TABLET, EXTENDED RELEASE | ORAL | 60MG | Prescription | AB2 | Yes |
| 003 | PROCARDIA XL | NIFEDIPINE | TABLET, EXTENDED RELEASE | ORAL | 90MG | Discontinued | not listed | Yes |
Product, form, strength, reference-drug and marketing-status fields: Drugs@FDA data files; TE and RLD fields: Orange Book data files. Retrieved 2026-08-07.
Orange Book patent and exclusivity listings
No Orange Book patent or exclusivity listings joined to this application.
Compound cross-links
- NIFEDIPINE · UNII I9ZF7L6G2L · lmmol compound HYIMSNHJOBLJNT-UHFFFAOYSA-N · CHEMBL193
Ingredient–compound links use FDA openFDA/GSRS identifiers and an exact lmmol InChIKey join. Ingredient names cannot create a link.
Related pages
Sponsor company · FDA-approved application index
Peer clusters: Large-cap biopharma
Sources: Drugs@FDA · Orange Book · openFDA application record. FDA data retrieved 2026-08-07.
Regulatory listing data as published by FDA; not medical or investment advice.