Prescription drug · ANDA
Amoxicillin NDC 0781-6039
Amoxicillin 125 mg/5mL · Powder, For suspension · Oral · Sandoz Inc
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0781-6039-46 | 00781603946 | 100 mL in 1 BOTTLE (0781-6039-46)Marketed from Mar 26, 2007 | |
| 0781-6039-55 | 00781603955 | 150 mL in 1 BOTTLE (0781-6039-55)Marketed from Mar 26, 2007 | |
| 0781-6039-58 | 00781603958 | 80 mL in 1 BOTTLE (0781-6039-58)Marketed from Mar 26, 2007 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
- Amoxicillin
- Generic name (nonproprietary)
- amoxicillin
- Active ingredients
- Amoxicillin — 125 mg/5mL
- Dosage form
- Powder, For suspension
- Route
- Oral
- Labeler
- Sandoz Inc
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 065387
- Marketing start
- Listing expires
- Other FDA classes
- Penicillins (Chemical structure)
- Identifiers
- Product ID 0781-6039_f4681ad2-fcc2-41f6-9100-90fb4524cd28SPL ID f4681ad2-fcc2-41f6-9100-90fb4524cd28SPL set ID 13bd4214-9b7f-425b-af5f-fc1ddc678230RxCUI 239191, 308182, 308189, 308191, 308192, 308194, 313797, 313850UNII 804826J2HUUPC 0307816156526, 0307812020012, 0307816041587, 0307815060015, 0307815061012, 0307816157523, 0307816039584, 0307812613016
- Pharmacologic class
- Penicillin-class 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
N400781603946followed by a unit qualifier and the quantityPackage 00781-6039-46. 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 065387
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 |
|---|---|---|---|---|
| Amoxicillin | Amoxicillin 250 mg/5mL | Powder, For suspensionOral | NuCare Pharmaceuticals,Inc. | 68071-4581 |
| Amoxicillin | Amoxicillin 250 mg/5mL | Powder, For suspensionOral | Sandoz Inc | 0781-6041 |
| Amoxicillin | Amoxicillin 125 mg/5mL | Powder, For suspensionOral | A-S Medication Solutions | 50090-6056 |
| Amoxicillin | Amoxicillin 250 mg/5mL | Powder, For suspensionOral | Proficient Rx LP | 63187-880 |
| Amoxicillin | Amoxicillin 125 mg/5mL | Powder, For suspensionOral | Preferred Pharmaceuticals, Inc. | 68788-9949 |
| Amoxicillin | Amoxicillin 250 mg/5mL | Powder, For suspensionOral | Preferred Pharmaceuticals, Inc. | 68788-9948 |
| Amoxicillin | Amoxicillin 125 mg/5mL | Powder, For suspensionOral | NuCare Pharmaceuticals,Inc. | 68071-4969 |
| Amoxicillin | Amoxicillin 125 mg/5mL | Powder, For suspensionOral | Proficient Rx LP | 71205-266 |
| Amoxicillin | Amoxicillin 125 mg/5mL | Powder, For suspensionOral | HAWAII REPACK, INC. | 85534-0070 |
| Amoxicillin | Amoxicillin 250 mg/5mL | Powder, For suspensionOral | HAWAII REPACK, INC. | 85534-0072 |