NDC codes

FDA NDC Directory
Product NDC (as listed)72252-505Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72252-0505Add 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
72252-505-0272252050502722520505022 BLISTER PACK in 1 CARTON (72252-505-02) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK / .1 mL in 1 VIAL, SINGLE-DOSEMarketed from Jan 10, 2020
72252-505-0572252050505722520505055 BLISTER PACK in 1 CARTON (72252-505-05) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK / .1 mL in 1 VIAL, SINGLE-DOSEMarketed from Feb 28, 2025

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)
Valtoco
Generic name (nonproprietary)
diazepam
Active ingredients
Diazepam — 5 mg/.1mL
Dosage form
Spray
Route
Nasal
Labeler
Neurelis, IncNDC labeler code 72252
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 211635
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 72252-505_6642d0cb-3186-4b4c-8a67-c3f92081fbd0SPL ID 6642d0cb-3186-4b4c-8a67-c3f92081fbd0SPL set ID 1a8bcc90-68fa-474d-832c-0df01e825f39RxCUI 2272613, 2272619, 2272621, 2272622, 2272623, 2272624, 2272626, 2272627, 2272629, 2272630, 2272632, 2272633, 2272635, 2272636UNII Q3JTX2Q7TU
Pharmacologic class
Benzodiazepine

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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N472252050502 followed by a unit qualifier and the quantity

Package 72252-0505-02. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

VALTOCO ® is indicated for the acute treatment of intermittent, stereotypic episodes of frequent seizure activity (i.e., seizure clusters, acute repetitive seizures) that are distinct from a patient's usual seizure pattern in patients with epilepsy 2 years of age and older. VALTOCO is a benzodiazepine indicated for the acute treatment of intermittent, stereotypic episodes of frequent seizure activity (i.e., seizure clusters, acute repetitive seizures) that are distinct from a patient's usual seizure pattern in patients with epilepsy 2 years of age and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72252-505

What is NDC 72252-505?
72252-505 is the product NDC for Valtoco (diazepam), Diazepam 5 mg/.1mL spray, listed with the FDA by Neurelis, Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Valtoco (Diazepam).
What is the active ingredient?
Diazepam.
Who is the labeler?
Neurelis, Inc, NDC labeler code 72252. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Valtoco?
3 other product NDCs are listed under this name. See all Valtoco NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Valtoco NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ValtocodiazepamDiazepam 10 mg/.1mLSprayNasalNeurelis, Inc72252-51072252-0510-0272252-0510-05
ValtocodiazepamDiazepam 7.5 mg/.1mLSprayNasalNeurelis, Inc72252-51572252-0515-0472252-0515-10
ValtocodiazepamDiazepam 10 mg/.1mLSprayNasalNeurelis, Inc72252-52072252-0520-0472252-0520-10

Other NDCs under NDA 211635

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

FDA NDC Directory listings under NDA 211635
ProductStrengthForm · routeLabelerProduct NDC
ValtocodiazepamDiazepam 10 mg/.1mLSprayNasalNeurelis, Inc72252-510
ValtocodiazepamDiazepam 7.5 mg/.1mLSprayNasalNeurelis, Inc72252-515
ValtocodiazepamDiazepam 10 mg/.1mLSprayNasalNeurelis, Inc72252-520

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