Prescription drug · ANDA
Methocarbamol NDC 71610-599
Methocarbamol 500 mg/1 · Tablet · Oral · Aphena Pharma Solutions - Tennessee, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71610-599-30 | 71610059930 | 30 TABLET in 1 BOTTLE (71610-599-30)Marketed from Sep 9, 2021 | |
| 71610-599-53 | 71610059953 | 60 TABLET in 1 BOTTLE (71610-599-53)Marketed from Sep 9, 2021 | |
| 71610-599-60 | 71610059960 | 90 TABLET in 1 BOTTLE (71610-599-60)Marketed from Sep 9, 2021 | |
| 71610-599-70 | 71610059970 | 120 TABLET in 1 BOTTLE (71610-599-70)Marketed from Oct 19, 2021 | |
| 71610-599-80 | 71610059980 | 180 TABLET in 1 BOTTLE (71610-599-80)Marketed from Sep 21, 2021 | |
| 71610-599-90 | 71610059990 | 240 TABLET in 1 BOTTLE (71610-599-90)Marketed from Sep 21, 2021 | |
| 71610-599-92 | 71610059992 | 270 TABLET in 1 BOTTLE (71610-599-92)Marketed from Sep 21, 2021 |
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)
- Methocarbamol
- Generic name (nonproprietary)
- methocarbamol
- Active ingredients
- Methocarbamol — 500 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Aphena Pharma Solutions - Tennessee, LLCNDC labeler code 71610
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 086989
- Marketing start
- Listing expires
- Other FDA classes
- Centrally-mediated Muscle Relaxation (Physiologic effect)
- Identifiers
- Product ID 71610-599_0d749d2c-80a9-4bc4-975e-cd9475de438aSPL ID 0d749d2c-80a9-4bc4-975e-cd9475de438aSPL set ID 27c39343-44e0-4ca6-a67f-1e6d11dd6799RxCUI 197943, 197944UNII 125OD7737X
- 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
N471610059930followed by a unit qualifier and the quantityPackage 71610-0599-30. 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 Methocarbamol tablets, USP are indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions. The mode of action of methocarbamol has not been clearly identified, but may be related to its sedative properties. Methocarbamol does not directly relax tense skeletal muscles in man.
Excerpt only. Read the full label for complete information.
About NDC 71610-599
- What is NDC 71610-599?
- 71610-599 is the product NDC for Methocarbamol, Methocarbamol 500 mg/1 tablet, listed with the FDA by Aphena Pharma Solutions - Tennessee, LLC. It has 7 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Methocarbamol.
- What is the active ingredient?
- Methocarbamol.
- Who is the labeler?
- Aphena Pharma Solutions - Tennessee, LLC, NDC labeler code 71610. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Methocarbamol?
- 197 other product NDCs are listed under this name. See all Methocarbamol NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Methocarbamol products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Methocarbamol | Methocarbamol 500 mg/1 | Tablet, Film coatedOral | St. Mary's Medical Park Pharmacy | 60760-874 | 60760-0874-90 |
| Methocarbamolmethocarbamol tablets | Methocarbamol 750 mg/1 | Tablet, CoatedOral | Coupler LLC | 67046-0340 | 67046-0340-03 |
| Methocarbamol | Methocarbamol 500 mg/1 | TabletOral | Coupler LLC | 67046-1177 | 67046-1177-03 |
| Methocarbamol | Methocarbamol 500 mg/1 | Tablet, Film coatedOral | Medcore LLC | 82461-722 | 82461-0722-90 |
| Methocarbamol | Methocarbamol 750 mg/1 | Tablet, Film coatedOral | Medcore LLC | 82461-723 | 82461-0723-90 |
| Methocarbamolmethocarbamol tablets | Methocarbamol 500 mg/1 | Tablet, CoatedOral | Unit Dose Solutions, Inc. | 87441-086 | 87441-0086-01 |
| Methocarbamol | Methocarbamol 750 mg/1 | Tablet, Film coatedOral | St. Mary's Medical Park Pharmacy | 60760-875 | 60760-0875-2860760-0875-4060760-0875-90 |
| Methocarbamol | Methocarbamol 500 mg/1 | TabletOral | Unit Dose Solutions, Inc. | 87441-057 | 87441-0057-01 |
| Methocarbamolmethocarbamol tablets | Methocarbamol 500 mg/1 | Tablet, CoatedOral | Coupler LLC | 67046-0538 | 67046-0538-03 |
| Methocarbamol | Methocarbamol 100 mg/mL | InjectionIntramuscular, Intravenous, Intravenous | JVET PHARMACEUTICALS LLC | 86211-114 | 86211-0114-10 |
Other NDCs under ANDA 086989
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 |
|---|---|---|---|---|
| Methocarbamol | Methocarbamol 500 mg/1 | TabletOral | Bryant Ranch Prepack | 63629-1123 |
| Methocarbamol | Methocarbamol 500 mg/1 | TabletOral | Proficient Rx LP | 71205-375 |
| Methocarbamol | Methocarbamol 500 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1795 |
| Methocarbamol | Methocarbamol 500 mg/1 | TabletOral | Bryant Ranch Prepack | 72162-1363 |