NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1795Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1795Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
71335-1795-07133517950015 TABLET in 1 BOTTLE (71335-1795-0)Marketed from Aug 27, 2021
71335-1795-17133517950114 TABLET in 1 BOTTLE (71335-1795-1)Marketed from Aug 27, 2021
71335-1795-27133517950230 TABLET in 1 BOTTLE (71335-1795-2)Marketed from Aug 27, 2021
71335-1795-37133517950320 TABLET in 1 BOTTLE (71335-1795-3)Marketed from Aug 27, 2021
71335-1795-47133517950460 TABLET in 1 BOTTLE (71335-1795-4)Marketed from Aug 27, 2021
71335-1795-571335179505100 TABLET in 1 BOTTLE (71335-1795-5)Marketed from Aug 27, 2021
71335-1795-67133517950640 TABLET in 1 BOTTLE (71335-1795-6)Marketed from Aug 27, 2021
71335-1795-77133517950790 TABLET in 1 BOTTLE (71335-1795-7)Marketed from Aug 27, 2021
71335-1795-871335179508120 TABLET in 1 BOTTLE (71335-1795-8)Marketed from Aug 27, 2021
71335-1795-9713351795097 TABLET in 1 BOTTLE (71335-1795-9)Marketed from Aug 27, 2021

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)
Methocarbamol
Generic name (nonproprietary)
methocarbamol
Active ingredients
Methocarbamol — 500 mg/1
Dosage form
Tablet
Route
Oral
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 71335-1795_fc9b729f-55ba-9df1-e053-6294a90a7d7cSPL ID fc9b729f-55ba-9df1-e053-6294a90a7d7cSPL set ID f1bce76f-4c3a-40d2-8107-afc0d3a6ba19RxCUI 197943UNII 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

N471335179500 followed by a unit qualifier and the quantity

Package 71335-1795-00. 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.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 086989

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 086989
ProductStrengthForm · routeLabelerProduct NDC
MethocarbamolMethocarbamol 500 mg/1TabletOralBryant Ranch Prepack72162-1363
MethocarbamolMethocarbamol 500 mg/1TabletOralBryant Ranch Prepack63629-1123
MethocarbamolMethocarbamol 500 mg/1TabletOralProficient Rx LP71205-375
MethocarbamolMethocarbamol 500 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-599

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