Prescription drug · NDA
Procardia XL (Nifedipine) NDC 0069-2650
Nifedipine 30 mg/1 · Tablet, Film coated, Extended release · Oral · Pfizer Laboratories Div Pfizer Inc
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0069-2650-41 | 0006926504100069265041 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0069-2650-41)Marketed from Sep 6, 1989 | |
| 0069-2650-66 | 0006926506600069265066 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2650-66)Marketed from Sep 6, 1989 | |
| 0069-2650-72 | 0006926507200069265072 | 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2650-72)Marketed from Sep 6, 1989 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Procardia XLSuffix: XL
- Generic name (nonproprietary)
- nifedipine
- Active ingredients
- Nifedipine — 30 mg/1
- Dosage form
- Tablet, Film coated, Extended release
- Route
- Oral
- Labeler
- Pfizer Laboratories Div Pfizer IncNDC labeler code 0069
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 019684
- Marketing start
- Listing expires
- Other FDA classes
- Calcium Channel Antagonists (Mechanism)Dihydropyridines (Chemical structure)
- Identifiers
- Product ID 0069-2650_adce4efa-91b5-4148-a893-efc66cf5ccb6SPL ID adce4efa-91b5-4148-a893-efc66cf5ccb6
- Pharmacologic class
- Dihydropyridine Calcium Channel Blocker
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N400069265041followed by a unit qualifier and the quantityPackage 00069-2650-41. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
The FDA listing for this product does not reference a label (SPL) set.
About NDC 0069-2650
- What is NDC 0069-2650?
- 0069-2650 is the product NDC for Procardia XL (nifedipine), Nifedipine 30 mg/1 tablet, film coated, extended release, listed with the FDA by Pfizer Laboratories Div Pfizer Inc. It has 3 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Procardia XL (Nifedipine).
- What is the active ingredient?
- Nifedipine.
- Who is the labeler?
- Pfizer Laboratories Div Pfizer Inc, NDC labeler code 0069. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Procardia XL?
- 1 other product NDC are listed under this name. See all Procardia XL NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Procardia XL products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Procardia XLnifedipine | Nifedipine 60 mg/1 | Tablet, Film coated, Extended releaseOral | Pfizer Laboratories Div Pfizer Inc | 0069-2660 | 00069-2660-4100069-2660-66 |
Other NDCs under NDA 019684
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Procardia XLnifedipine | Nifedipine 60 mg/1 | Tablet, Film coated, Extended releaseOral | Pfizer Laboratories Div Pfizer Inc | 0069-2660 |