Prescription drug · ANDA
Cyclobenzaprine Hydrochloride (Cyclobenzaprine) NDC 68071-3150
Cyclobenzaprine hydrochloride 10 mg/1 · Tablet, Film coated · Oral · NuCare Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68071-3150-1 | 6807131500168071315001 | 21 TABLET, FILM COATED in 1 BOTTLE (68071-3150-1)Marketed from Mar 7, 2017 | |
| 68071-3150-2 | 6807131500268071315002 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-3150-2)Marketed from Mar 7, 2017 | |
| 68071-3150-3 | 6807131500368071315003 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3150-3)Marketed from Mar 7, 2017 | |
| 68071-3150-4 | 6807131500468071315004 | 84 TABLET, FILM COATED in 1 BOTTLE (68071-3150-4)Marketed from Mar 16, 2017 | |
| 68071-3150-5 | 6807131500568071315005 | 15 TABLET, FILM COATED in 1 BOTTLE (68071-3150-5)Marketed from Mar 7, 2017 | |
| 68071-3150-6 | 6807131500668071315006 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-3150-6)Marketed from Mar 7, 2017 | |
| 68071-3150-7 | 6807131500768071315007 | 7 TABLET, FILM COATED in 1 BOTTLE (68071-3150-7)Marketed from Mar 7, 2017 | |
| 68071-3150-8 | 6807131500868071315008 | 6 TABLET, FILM COATED in 1 BOTTLE (68071-3150-8)Marketed from Mar 7, 2017 | |
| 68071-3150-9 | 6807131500968071315009 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3150-9)Marketed from Mar 7, 2017 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
- Cyclobenzaprine Hydrochloride
- Generic name (nonproprietary)
- cyclobenzaprine
- Active ingredients
- Cyclobenzaprine hydrochloride — 10 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- NuCare Pharmaceuticals, Inc.NDC labeler code 68071
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090478
- Marketing start
- Listing expires
- Other FDA classes
- Centrally-mediated Muscle Relaxation (Physiologic effect)
- Identifiers
- Product ID 68071-3150_51171bd5-4e45-8084-e063-6294a90a6f71SPL ID 51171bd5-4e45-8084-e063-6294a90a6f71SPL set ID 4a2b5f25-a333-15f3-e054-00144ff8d46cRxCUI 828348UNII 0VE05JYS2PUPC 0368071315035
- Pharmacologic class
- Muscle Relaxant
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
N468071315001followed by a unit qualifier and the quantityPackage 68071-3150-01. 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)
INDICATIONS AND USAGE Cyclobenzaprine HCl tablets USP are indicated as an adjunct to rest and physical therapy for relief of muscle spasm associated with acute, painful musculoskeletal conditions. Improvement is manifested by relief of muscle spasm and its associated signs and symptoms, namely, pain, tenderness, limitation of motion, and restriction in activities of daily living. Cyclobenzaprine HCl should be used only for short periods (up to two or three weeks) because adequate evidence of effectiveness for more prolonged use is not available and because muscle spasm associated with acute, painful musculoskeletal conditions is generally of short duration and specific therapy for longer per…
Excerpt only. Read the full label for complete information.
About NDC 68071-3150
- What is NDC 68071-3150?
- 68071-3150 is the product NDC for Cyclobenzaprine Hydrochloride (cyclobenzaprine), Cyclobenzaprine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by NuCare Pharmaceuticals, Inc.. It has 9 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Cyclobenzaprine Hydrochloride (Cyclobenzaprine).
- What is the active ingredient?
- Cyclobenzaprine hydrochloride.
- Who is the labeler?
- NuCare Pharmaceuticals, Inc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Cyclobenzaprine Hydrochloride?
- 221 other product NDCs are listed under this name. See all Cyclobenzaprine Hydrochloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Cyclobenzaprine 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) |
|---|---|---|---|---|---|
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine hydrochloride 7.5 mg/1 | Tablet, Film coatedOral | Carol Way Pharma LLC | 85437-013 | 85437-0013-10 |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine hydrochloride 7.5 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4751 | 70518-4751-00 |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-4154 | 68788-4154-0268788-4154-0368788-4154-05+2 more |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine hydrochloride 10 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4692 | 70518-4692-0070518-4692-0170518-4692-02 |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Unit Dose Solutions, Inc. | 87441-010 | 87441-0010-01 |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine hydrochloride 5 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1110 | 67046-1110-03 |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine hydrochloride 15 mg/1 | Capsule, Extended releaseOral | Preferred Pharmaceuticals Inc. | 68788-4087 | 68788-4087-0368788-4087-06 |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine hydrochloride 5 mg/1 | Tablet, Film coatedOral | Medcore LLC | 82461-714 | 82461-0714-90 |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Medcore LLC | 82461-716 | 82461-0716-90 |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1645 | 67046-1645-03 |
Other NDCs under ANDA 090478
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 |
|---|---|---|---|---|
| Cyclobenzaprine Hydrochloridecyclobenzaprine | Cyclobenzaprine hydrochloride 10 mg/1 | TabletOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-933 |
| Cyclobenzaprine Hydrochloridecyclobenzaprine | Cyclobenzaprine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-973 |
| Cyclobenzaprine Hydrochloridecyclobenzaprine | Cyclobenzaprine hydrochloride 10 mg/1 | Tablet, Film coatedOral | American Health Packaging | 60687-558 |
| Cyclobenzaprine Hydrochloridecyclobenzaprine | Cyclobenzaprine hydrochloride 10 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals, Inc. | 68071-3154 |
| Cyclobenzaprine Hydrochloridecyclobenzaprine | Cyclobenzaprine hydrochloride 10 mg/1 | TabletOral | EXELAN PHARMACEUTICALS, INC. | 76282-283 |
| Cyclobenzaprine Hydrochloridecyclobenzaprine | Cyclobenzaprine hydrochloride 5 mg/1 | Tablet, Film coatedOral | Cipla USA Inc. | 69097-845 |
| Cyclobenzaprine Hydrochloridecyclobenzaprine | Cyclobenzaprine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Cipla USA Inc. | 69097-846 |
| Cyclobenzaprine Hydrochloridecyclobenzaprine | Cyclobenzaprine hydrochloride 10 mg/1 | Tablet, Film coatedOral | NCS HealthCare of KY, LLC dba Vangard Labs | 0615-8084 |
| Cyclobenzaprine Hydrochloridecyclobenzaprine | Cyclobenzaprine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 63187-812 |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine hydrochloride 5 mg/1 | Tablet, Film coatedOral | AvPAK | 50268-190 |
| Cyclobenzaprine Hydrochloridecyclobenzaprine | Cyclobenzaprine hydrochloride 10 mg/1 | Tablet, Film coatedOral | AvPAK | 50268-191 |