Prescription drug · ANDA
Bimatoprost NDC 72266-140
Bimatoprost .3 mg/mL · Solution/ drops · Ophthalmic · Fosun Pharma USA Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72266-140-01 | 72266014001 | 1 BOTTLE in 1 CARTON (72266-140-01) / 5 mL in 1 BOTTLEMarketed from Aug 10, 2020 |
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)
- Bimatoprost
- Generic name (nonproprietary)
- bimatoprost
- Active ingredients
- Bimatoprost — .3 mg/mL
- Dosage form
- Solution/ drops
- Route
- Ophthalmic
- Labeler
- Fosun Pharma USA Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 210126
- Marketing start
- Listing expires
- Other FDA classes
- Prostaglandins (Chemical structure)
- Identifiers
- Product ID 72266-140_2c7970dc-8873-7e74-e063-6294a90a397fSPL ID 2c7970dc-8873-7e74-e063-6294a90a397fSPL set ID 2f9ee30a-1737-44b2-8479-79a3ee88bf5bRxCUI 308739UNII QXS94885MZ
- Pharmacologic class
- Prostaglandin Analog
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. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N472266014001followed by a unit qualifier and the quantityPackage 72266-0140-01. 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 210126
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 |
|---|---|---|---|---|
| Bimatoprost | Bimatoprost .3 mg/mL | Solution/ dropsOphthalmic | Fosun Pharma USA Inc. | 72266-139 |
| Bimatoprost | Bimatoprost .3 mg/mL | Solution/ dropsOphthalmic | NuCare Pharmaceuticals,Inc. | 68071-3590 |
| Bimatoprost | Bimatoprost .3 mg/mL | Solution/ dropsOphthalmic | Fosun Pharma USA Inc. | 72266-241 |
| Bimatoprost | Bimatoprost .3 mg/mL | Solution/ dropsOphthalmic | Gland Pharma Limited | 68083-295 |
| Bimatoprost | Bimatoprost .3 mg/mL | Solution/ dropsOphthalmic | Gland Pharma Limited | 68083-296 |
| Bimatoprost | Bimatoprost .3 mg/mL | Solution/ dropsOphthalmic | Gland Pharma Limited | 68083-439 |