Prescription drug · ANDA
Prednisolone Acetate NDC 70748-332
Prednisolone acetate 10 mg/mL · Suspension/ drops · Ophthalmic · Lupin Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70748-332-02 | 70748033202 | 1 BOTTLE in 1 CARTON (70748-332-02) / 5 mL in 1 BOTTLEMarketed from Oct 11, 2024 | |
| 70748-332-03 | 70748033203 | 1 BOTTLE in 1 CARTON (70748-332-03) / 10 mL in 1 BOTTLEMarketed from Oct 11, 2024 | |
| 70748-332-04 | 70748033204 | 1 BOTTLE in 1 CARTON (70748-332-04) / 15 mL in 1 BOTTLEMarketed from Oct 11, 2024 |
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)
- Prednisolone Acetate
- Generic name (nonproprietary)
- prednisolone acetate
- Active ingredients
- Prednisolone acetate — 10 mg/mL
- Dosage form
- Suspension/ drops
- Route
- Ophthalmic
- Labeler
- Lupin Pharmaceuticals, Inc.NDC labeler code 70748
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 216935
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 70748-332_8b7144d6-fff1-4afd-a80b-332ff7ed80a1SPL ID 8b7144d6-fff1-4afd-a80b-332ff7ed80a1SPL set ID 75fbeab1-ce8d-4999-a875-472174be5cc6RxCUI 1376336UNII 8B2807733D
- Pharmacologic class
- Corticosteroid
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
N470748033202followed by a unit qualifier and the quantityPackage 70748-0332-02. 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 Prednisolone acetate ophthalmic suspension is indicated for the treatment of steroid-responsive inflammation of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the globe.
Excerpt only. Read the full label for complete information.
About NDC 70748-332
- What is NDC 70748-332?
- 70748-332 is the product NDC for Prednisolone Acetate, Prednisolone acetate 10 mg/mL suspension/ drops, listed with the FDA by Lupin Pharmaceuticals, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Prednisolone Acetate.
- What is the active ingredient?
- Prednisolone acetate.
- Who is the labeler?
- Lupin Pharmaceuticals, Inc., NDC labeler code 70748. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Prednisolone Acetate?
- 14 other product NDCs are listed under this name. See all Prednisolone Acetate NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Prednisolone Acetate products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| prednisolone acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | Amneal Pharmaceuticals NY LLC | 60219-2550 | 60219-2550-01 |
| prednisolone acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | Amneal Pharmaceuticals NY LLC | 60219-2551 | 60219-2551-01 |
| prednisolone acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | Amneal Pharmaceuticals NY LLC | 60219-2552 | 60219-2552-01 |
| Prednisolone Acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | Redpharm Drug | 67296-2176 | 67296-2176-05 |
| Prednisolone Acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | A-S Medication Solutions | 50090-7539 | 50090-7539-00 |
| Prednisolone Acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | A-S Medication Solutions | 50090-5275 | 50090-5275-00 |
| Prednisolone Acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | NuCare Pharmaceuticals,Inc. | 68071-2222 | 68071-2222-05 |
| Prednisolone Acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | A-S Medication Solutions | 50090-1912 | 50090-1912-00 |
| Prednisolone Acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | Sportpharm LLC | 85766-124 | 85766-0124-05 |
| Prednisolone Acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | Asclemed USA, Inc. | 76420-204 | 76420-0204-05 |
Other NDCs under ANDA 216935
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 |
|---|---|---|---|---|
| Prednisolone Acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | Redpharm Drug | 67296-2176 |
| Prednisolone Acetate | Prednisolone acetate 10 mg/mL | Suspension/ dropsOphthalmic | A-S Medication Solutions | 50090-7539 |