Prescription drug · NDA AUTHORIZED GENERIC
Diltiazem Hydrochloride NDC 68682-006
Diltiazem hydrochloride 30 mg/1 · Tablet · Oral · Oceanside Pharmaceuticals
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68682-006-10 | 6868200061068682000610 | 100 TABLET in 1 BOTTLE (68682-006-10)Marketed from Dec 25, 2010 | |
| 68682-006-50 | 6868200065068682000650 | 500 TABLET in 1 BOTTLE (68682-006-50)Marketed from Dec 25, 2010 |
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)
- Diltiazem Hydrochloride
- Generic name (nonproprietary)
- diltiazem hydrochloride
- Active ingredients
- Diltiazem hydrochloride — 30 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Oceanside PharmaceuticalsNDC labeler code 68682
- Product type
- Prescription drug
- Marketing category
- NDA authorized genericApplication NDA 018602
- Marketing start
- Listing expires
- Other FDA classes
- Calcium Channel Antagonists (Mechanism)
- Identifiers
- Product ID 68682-006_06626a5d-987f-4d1c-9ffc-28fd51362900SPL ID 06626a5d-987f-4d1c-9ffc-28fd51362900SPL set ID f6a24de7-8ffe-48af-873f-10fdcd5551d1RxCUI 831054, 831102, 831103, 833217UNII OLH94387TEUPC 0368682006100, 0368682009101, 0368682008104, 0368682007107
- Pharmacologic class
- Calcium Channel Blocker
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
N468682000610followed by a unit qualifier and the quantityPackage 68682-0006-10. 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 Diltiazem hydrochloride tablets are indicated for the management of chronic stable angina and angina due to coronary artery spasm.
Excerpt only. Read the full label for complete information.
About NDC 68682-006
- What is NDC 68682-006?
- 68682-006 is the product NDC for Diltiazem Hydrochloride, Diltiazem hydrochloride 30 mg/1 tablet, listed with the FDA by Oceanside Pharmaceuticals. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Diltiazem Hydrochloride.
- What is the active ingredient?
- Diltiazem hydrochloride.
- Who is the labeler?
- Oceanside Pharmaceuticals, NDC labeler code 68682. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Diltiazem Hydrochloride?
- 223 other product NDCs are listed under this name. See all Diltiazem Hydrochloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Diltiazem Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Diltiazem Hydrochloride | Diltiazem hydrochloride 60 mg/1 | Capsule, Extended releaseOral | Cranbury Pharmaceuticals, LLC | 27808-322 | 27808-0322-01 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 90 mg/1 | Capsule, Extended releaseOral | Cranbury Pharmaceuticals, LLC | 27808-323 | 27808-0323-01 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 120 mg/1 | Capsule, Extended releaseOral | Cranbury Pharmaceuticals, LLC | 27808-324 | 27808-0324-01 |
| Diltiazem hydrochloride | Diltiazem hydrochloride 30 mg/1 | TabletOral | Zydus Lifesciences Limited | 70771-1929 | 70771-1929-0170771-1929-05 |
| Diltiazem hydrochloride | Diltiazem hydrochloride 60 mg/1 | TabletOral | Zydus Lifesciences Limited | 70771-1930 | 70771-1930-0170771-1930-05 |
| Diltiazem hydrochloride | Diltiazem hydrochloride 90 mg/1 | TabletOral | Zydus Lifesciences Limited | 70771-1931 | 70771-1931-0170771-1931-05 |
| Diltiazem hydrochloride | Diltiazem hydrochloride 120 mg/1 | TabletOral | Zydus Lifesciences Limited | 70771-1932 | 70771-1932-0170771-1932-05 |
| Diltiazem hydrochloride | Diltiazem hydrochloride 30 mg/1 | TabletOral | Viona Pharmaceuticals Inc | 72578-199 | 72578-0199-0172578-0199-05 |
| Diltiazem hydrochloride | Diltiazem hydrochloride 60 mg/1 | TabletOral | Viona Pharmaceuticals Inc | 72578-200 | 72578-0200-0172578-0200-05 |
| Diltiazem hydrochloride | Diltiazem hydrochloride 90 mg/1 | TabletOral | Viona Pharmaceuticals Inc | 72578-201 | 72578-0201-0172578-0201-05 |
Other NDCs under NDA 018602
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 |
|---|---|---|---|---|
| Cardizemdiltiazem hydrochloride | Diltiazem hydrochloride 30 mg/1 | Tablet, CoatedOral | Bausch Health US LLC | 0187-0771 |
| Cardizemdiltiazem hydrochloride | Diltiazem hydrochloride 60 mg/1 | Tablet, CoatedOral | Bausch Health US LLC | 0187-0772 |
| Cardizemdiltiazem hydrochloride | Diltiazem hydrochloride 120 mg/1 | Tablet, CoatedOral | Bausch Health US LLC | 0187-0792 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 120 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-4242 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 60 mg/1 | TabletOral | Oceanside Pharmaceuticals | 68682-007 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 90 mg/1 | TabletOral | Oceanside Pharmaceuticals | 68682-008 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 120 mg/1 | TabletOral | Oceanside Pharmaceuticals | 68682-009 |
| Diltiazem Hydrochloride | Diltiazem hydrochloride 90 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-0579 |