Prescription drug · ANDA
budesonide NDC 68382-720
Budesonide 3 mg/1 · Capsule, Coated pellets · Oral · Zydus Pharmaceuticals USA Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68382-720-01 | 68382072001 | 100 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-01)Marketed from Jun 8, 2017 | |
| 68382-720-05 | 68382072005 | 500 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-05)Marketed from Jun 8, 2017 | |
| 68382-720-06 | 68382072006 | 30 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-06)Marketed from Jun 8, 2017 | |
| 68382-720-10 | 68382072010 | 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-10)Marketed from Jun 8, 2017 | |
| 68382-720-16 | 68382072016 | 90 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-720-16)Marketed from Jun 8, 2017 | |
| 68382-720-77 | 68382072077 | 10 BLISTER PACK in 1 CARTON (68382-720-77) / 10 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68382-720-30)Marketed from Jun 8, 2017 |
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)
- budesonide
- Generic name (nonproprietary)
- budesonide
- Active ingredients
- Budesonide — 3 mg/1
- Dosage form
- Capsule, Coated pellets
- Route
- Oral
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 206134
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 68382-720_08f8aa4f-4543-46d3-91f7-ae943f455648SPL ID 08f8aa4f-4543-46d3-91f7-ae943f455648SPL set ID 29863154-5f98-410e-9bf3-0f08b551edefRxCUI 1244214UNII Q3OKS62Q6XUPC 0368382720016
- 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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N468382072001followed by a unit qualifier and the quantityPackage 68382-0720-01. 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
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Budesonide delayed-release capsules are corticosteroid indicated for: Treatment of mild to moderate active Crohn's disease involving the ileum and/or the ascending colon, in patients 8 years and older. ( 1.1 ) Maintenance of clinical remission of mild to moderate Crohn's disease involving the ileum and/or the ascending colon for up to 3 months in adults. ( 1.2 ) 1.1 Treatment of Mild to Moderate Active Crohn’s Disease Budesonide delayed-release capsules are indicated for the treatment of mild to moderate active Crohn's disease involving the ileum and/or the ascending colon in patients 8 years of age and older. 1.2 Maintenance of Clinical Remission of Mild to Moderate Crohn’s Disease Budesoni…
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 206134
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 |
|---|---|---|---|---|
| budesonide | Budesonide 3 mg/1 | Capsule, Coated pelletsOral | Zydus Lifesciences Limited | 70771-1075 |
| budesonide | Budesonide 3 mg/1 | Capsule, Coated pelletsOral | Northstar Rx LLC. | 16714-829 |
| Budesonide | Budesonide 3 mg/1 | Capsule, Coated pelletsOral | American Health Packaging | 60687-596 |
| budesonide | Budesonide 3 mg/1 | Capsule, Coated pelletsOral | Major Pharmaceuticals | 0904-7313 |
| budesonide | Budesonide 3 mg/1 | Capsule, Coated pelletsOral | REMEDYREPACK INC. | 70518-4613 |