Prescription drug · ANDA
Cycloserine NDC 43598-235
Cycloserine 250 mg/1 · Capsule · Oral · Dr. Reddys Laboratories, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 43598-235-31 | 4359802353143598023531 | 3 BLISTER PACK in 1 CARTON (43598-235-31) / 10 CAPSULE in 1 BLISTER PACK (43598-235-10)Marketed from Mar 15, 2023 |
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)
- Cycloserine
- Generic name (nonproprietary)
- cycloserine
- Active ingredients
- Cycloserine — 250 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- Dr. Reddys Laboratories, Inc.NDC labeler code 43598
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 060593
- Marketing start
- Listing expires
- Identifiers
- Product ID 43598-235_426b2c99-759d-647a-420f-fc11b205486bSPL ID 426b2c99-759d-647a-420f-fc11b205486bSPL set ID 8e7e2665-7a3d-3f54-9f92-5fe845f02ef9RxCUI 197551UNII 95IK5KI84Z
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
N443598023531followed by a unit qualifier and the quantityPackage 43598-0235-31. 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
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE Cycloserine is indicated in the treatment of active pulmonary and extrapulmonary tuberculosis (including renal disease) when the causative organisms are susceptible to this drug and when treatment with the primary medications (streptomycin, isoniazid, rifampin, and ethambutol) has proved inadequate. Like all antituberculosis drugs, cycloserine should be administered in conjunction with other effective chemotherapy and not as the sole therapeutic agent. Cycloserine may be effective in the treatment of acute urinary tract infections caused by susceptible strains of gram-positive and gram- negative bacteria. Use of cycloserine in these infections should be considered only …
Excerpt only. Read the full label for complete information.
About NDC 43598-235
- What is NDC 43598-235?
- 43598-235 is the product NDC for Cycloserine, Cycloserine 250 mg/1 capsule, listed with the FDA by Dr. Reddys Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Cycloserine.
- What is the active ingredient?
- Cycloserine.
- Who is the labeler?
- Dr. Reddys Laboratories, Inc., NDC labeler code 43598. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Cycloserine?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.