Prescription drug · ANDA
Eletriptan hydrobromide NDC 31722-443
Eletriptan hydrobromide 20 mg/1 · Tablet, Film coated · Oral · Camber Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 31722-443-31 | 31722044331 | 1 BLISTER PACK in 1 CARTON (31722-443-31) / 6 TABLET, FILM COATED in 1 BLISTER PACK (31722-443-32)Marketed from Jul 7, 2025 |
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)
- Eletriptan hydrobromide
- Generic name (nonproprietary)
- eletriptan hydrobromide
- Active ingredients
- Eletriptan hydrobromide — 20 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Camber Pharmaceuticals, Inc.NDC labeler code 31722
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 219143
- Marketing start
- Listing expires
- Other FDA classes
- Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
- Identifiers
- Product ID 31722-443_3d920aff-46bc-82ae-e063-6294a90a4222SPL ID 3d920aff-46bc-82ae-e063-6294a90a4222SPL set ID 6d412c0d-c8bd-498d-b57c-6626fb33147aRxCUI 359493, 359494UNII M41W832TA3
- Pharmacologic class
- Serotonin-1b and Serotonin-1d Receptor Agonist
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
N431722044331followed by a unit qualifier and the quantityPackage 31722-0443-31. 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)
Eletriptan hydrobromide tablets are indicated for the acute treatment of migraine with or without aura in adults. Limitations of Use: • Use only if a clear diagnosis of migraine has been established. If a patient has no response to the first migraine attack treated with eletriptan hydrobromide tablets, reconsider the diagnosis of migraine before eletriptan hydrobromide tablets are administered to treat any subsequent attacks. • Eletriptan hydrobromide tablets are not intended for the prevention of migraine attacks. • Safety and effectiveness of eletriptan hydrobromide tablets have not been established for cluster headache. Eletriptan hydrobromide tablets are a serotonin (5-HT 1B/1D ) recepto…
Excerpt only. Read the full label for complete information.
About NDC 31722-443
- What is NDC 31722-443?
- 31722-443 is the product NDC for Eletriptan hydrobromide, Eletriptan hydrobromide 20 mg/1 tablet, film coated, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Eletriptan hydrobromide.
- What is the active ingredient?
- Eletriptan hydrobromide.
- Who is the labeler?
- Camber Pharmaceuticals, Inc., NDC labeler code 31722. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Eletriptan hydrobromide?
- 16 other product NDCs are listed under this name. See all Eletriptan hydrobromide NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Eletriptan hydrobromide products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Eletriptan Hydrobromide | Eletriptan hydrobromide 20 mg/1 | Tablet, Film coatedOral | Apnar Pharma LP | 24689-167 | 24689-0167-01 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Apnar Pharma LP | 24689-168 | 24689-0168-01 |
| Eletriptan hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Camber Pharmaceuticals, Inc. | 31722-444 | 31722-0444-3131722-0444-33 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Advanced Rx of Tennessee, LLC | 80425-0408 | 80425-0408-01 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 20 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-104 | 59651-0104-69 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 59651-105 | 59651-0105-6959651-0105-93 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 63629-8320 | 63629-8320-0163629-8320-02 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 20 mg/1 | Tablet, Film coatedOral | Mylan Pharmaceuticals Inc. | 0378-4287 | 00378-4287-85 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Mylan Pharmaceuticals Inc. | 0378-4288 | 00378-4288-0800378-4288-85 |
| Eletriptan Hydrobromide | Eletriptan hydrobromide 20 mg/1 | Tablet, Film coatedOral | Teva Pharmaceuticals USA, Inc. | 0093-8310 | 00093-8310-18 |
Other NDCs under ANDA 219143
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 |
|---|---|---|---|---|
| Eletriptan hydrobromide | Eletriptan hydrobromide 40 mg/1 | Tablet, Film coatedOral | Camber Pharmaceuticals, Inc. | 31722-444 |