Prescription drug · ANDA
Modafinil NDC 68071-5121
Modafinil 100 mg/1 · Tablet · Oral · NuCare Pharmaceuticals,Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68071-5121-3 | 68071512103 | 30 TABLET in 1 BOTTLE (68071-5121-3)Marketed from Dec 4, 2019 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
- Modafinil
- Generic name (nonproprietary)
- modafinil
- Active ingredients
- Modafinil — 100 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- NuCare Pharmaceuticals,Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 202566
- Marketing start
- Listing expires
- DEA schedule
- CIV
- Other FDA classes
- Central Nervous System Stimulation (Physiologic effect)Increased Sympathetic Activity (Physiologic effect)
- Identifiers
- Product ID 68071-5121_1b547633-2137-67d7-e063-6294a90a1b5aSPL ID 1b547633-2137-67d7-e063-6294a90a1b5aSPL set ID 98e54b10-8ae0-7c43-e053-2a95a90ae8bbRxCUI 260218UNII R3UK8X3U3DUPC 0368071512137
- Pharmacologic class
- Sympathomimetic-like Agent
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
N468071512103followed by a unit qualifier and the quantityPackage 68071-5121-03. 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)
Modafinil tablets, USP are indicated to improve wakefulness in adult patients with excessive sleepiness associated with narcolepsy, obstructive sleep apnea (OSA), or shift work disorder (SWD). Limitations of Use In OSA, modafinil tablets, USP are indicated to treat excessive sleepiness and not as treatment for the underlying obstruction. If continuous positive airway pressure (CPAP) is the treatment of choice for a patient, a maximal effort to treat with CPAP for an adequate period of time should be made prior to initiating and during treatment with modafinil tablets, USP for excessive sleepiness. Modafinil tablets, USP are indicated to improve wakefulness in adult patients with excessive sl…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 202566
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 |
|---|---|---|---|---|
| Modafinil | Modafinil 100 mg/1 | TabletOral | Aurobindo Pharma Limited | 65862-601 |
| Modafinil | Modafinil 200 mg/1 | TabletOral | Proficient Rx LP | 71205-544 |
| Modafinil | Modafinil 200 mg/1 | TabletOral | Aurobindo Pharma Limited | 65862-602 |
| Modafinil | Modafinil 200 mg/1 | TabletOral | ASCLEMED USA INC. | 87063-307 |
| Modafinil | Modafinil 100 mg/1 | TabletOral | ASCLEMED USA INC. | 87063-306 |
| Modafinil | Modafinil 100 mg/1 | TabletOral | AvPAK | 50268-570 |
| Modafinil | Modafinil 200 mg/1 | TabletOral | AvPAK | 50268-571 |
| Modafinil | Modafinil 100 mg/1 | TabletOral | American Health Packaging | 68084-621 |
| Modafinil | Modafinil 200 mg/1 | TabletOral | American Health Packaging | 68084-721 |
| Modafinil | Modafinil 100 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1122 |
| Modafinil | Modafinil 100 mg/1 | TabletOral | Proficient Rx LP | 71205-477 |
| Modafinil | Modafinil 200 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1173 |
| Modafinil | Modafinil 200 mg/1 | TabletOral | Bryant Ranch Prepack | 63629-7315 |
| Modafinil | Modafinil 100 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 57237-154 |
| Modafinil | Modafinil 200 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 57237-155 |