Prescription drug · ANDA
Nitrofurantion NDC 68001-385
Nitrofurantoin 50 mg/1 · Capsule · Oral · BluePoint Labortories
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68001-385-00 | 6800103850068001038500 | 100 CAPSULE in 1 BOTTLE (68001-385-00)Marketed from May 14, 2019 |
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)
- Nitrofurantion
- Generic name (nonproprietary)
- nitrofurantion
- Active ingredients
- Nitrofurantoin — 50 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- BluePoint LabortoriesNDC labeler code 68001
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 201722
- Marketing start
- Listing expires
- Other FDA classes
- Nitrofurans (Chemical structure)
- Identifiers
- Product ID 68001-385_ad020393-1c97-49da-b0f3-d6a9359fb73dSPL ID ad020393-1c97-49da-b0f3-d6a9359fb73dSPL set ID ad020393-1c97-49da-b0f3-d6a9359fb73dRxCUI 311994, 311995, 1648759UNII 927AH8112LUPC 0368001385008, 0368001386005
- Pharmacologic class
- Nitrofuran Antibacterial
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
N468001038500followed by a unit qualifier and the quantityPackage 68001-0385-00. 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: Nitrofurantoin Capsules, USP (macrocrystals) is specifically indicated for the treatment of urinary tract infections when due to susceptible strains of Escherichia coli, enterococci, Staphylococcus aureus, and certain susceptible strains of Klebsiella and Enterobacter species. Nitrofurantoin is not indicated for the treatment of pyelonephritis or perinephric abscesses. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Nitrofurantoin Capsules, USP (macrocrystals) and other antibacterial drugs, Nitrofurantoin Capsules, USP (macrocrystals) should be used only to treat or prevent infections that are proven or strongly suspected to be ca…
Excerpt only. Read the full label for complete information.
About NDC 68001-385
- What is NDC 68001-385?
- 68001-385 is the product NDC for Nitrofurantion, Nitrofurantoin 50 mg/1 capsule, listed with the FDA by BluePoint Labortories. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Nitrofurantion.
- What is the active ingredient?
- Nitrofurantoin.
- Who is the labeler?
- BluePoint Labortories, NDC labeler code 68001. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Nitrofurantion?
- 9 other product NDCs are listed under this name. See all Nitrofurantion NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Nitrofurantion products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Nitrofurantion | Nitrofurantoin 25 mg/1 | CapsuleOral | BluePoint Labortories | 68001-384 | 68001-0384-00 |
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | BluePoint Labortories | 68001-386 | 68001-0386-00 |
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-5693 | 50090-5693-0050090-5693-0250090-5693-03 |
| Nitrofurantion | Nitrofurantoin 25 mg/1 | CapsuleOral | Sun Pharmaceutical Industries, Inc. | 57664-231 | 57664-0231-1857664-0231-88 |
| Nitrofurantion | Nitrofurantoin 50 mg/1 | CapsuleOral | Sun Pharmaceutical Industries, Inc. | 57664-232 | 57664-0232-1857664-0232-88 |
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | Sun Pharmaceutical Industries, Inc. | 57664-233 | 57664-0233-1857664-0233-88 |
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | NuCare Pharmaceuticals,Inc. | 68071-2363 | 68071-2363-0768071-2363-08 |
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | Proficient Rx LP | 71205-171 | 71205-0171-1071205-0171-1471205-0171-20+1 more |
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | Bryant Ranch Prepack | 71335-0024 | 71335-0024-0171335-0024-0271335-0024-03+6 more |
Other NDCs under ANDA 201722
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 |
|---|---|---|---|---|
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | A-S Medication Solutions | 50090-5693 |
| Nitrofurantion | Nitrofurantoin 25 mg/1 | CapsuleOral | Sun Pharmaceutical Industries, Inc. | 57664-231 |
| Nitrofurantion | Nitrofurantoin 50 mg/1 | CapsuleOral | Sun Pharmaceutical Industries, Inc. | 57664-232 |
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | Sun Pharmaceutical Industries, Inc. | 57664-233 |
| Nitrofurantion | Nitrofurantoin 25 mg/1 | CapsuleOral | BluePoint Labortories | 68001-384 |
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | BluePoint Labortories | 68001-386 |
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | NuCare Pharmaceuticals,Inc. | 68071-2363 |
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | Proficient Rx LP | 71205-171 |
| Nitrofurantion | Nitrofurantoin 100 mg/1 | CapsuleOral | Bryant Ranch Prepack | 71335-0024 |