Prescription drug · ANDA
Chlorthalidone NDC 83980-062
Chlorthalidone 50 mg/1 · Tablet · Oral · Ipca Laboratories Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 83980-062-01 | 83980006201 | 100 TABLET in 1 BOTTLE (83980-062-01)Marketed from Sep 21, 2026 | |
| 83980-062-10 | 83980006210 | 1000 TABLET in 1 BOTTLE (83980-062-10)Marketed from Sep 21, 2026 | |
| 83980-062-13 | 83980006213 | 30 TABLET in 1 BOTTLE (83980-062-13)Marketed from Sep 21, 2026 | |
| 83980-062-19 | 83980006219 | 90 TABLET in 1 BOTTLE (83980-062-19)Marketed from Sep 21, 2026 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
- Chlorthalidone
- Generic name (nonproprietary)
- chlorthalidone
- Active ingredients
- Chlorthalidone — 50 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Ipca Laboratories Limited
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 209162
- Marketing start
- Listing expires
- Other FDA classes
- Increased Diuresis (Physiologic effect)
- Identifiers
- Product ID 83980-062_b1a9b0ed-396f-41cc-b975-349b61b99d14SPL ID b1a9b0ed-396f-41cc-b975-349b61b99d14
- Pharmacologic class
- Thiazide-like Diuretic
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
N483980006201followed by a unit qualifier and the quantityPackage 83980-0062-01. 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.
Other NDCs under ANDA 209162
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 |
|---|---|---|---|---|
| Chlorthalidone | Chlorthalidone 25 mg/1 | TabletOral | Ipca Laboratories Limited | 83980-061 |