NDC codes

FDA NDC Directory
Product NDC (as listed)70710-1850Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70710-1850Add 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
70710-1850-77071018500725 VIAL in 1 CARTON (70710-1850-7) / 2 mL in 1 VIAL (70710-1850-1)Marketed from Mar 29, 2024

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)
Chlorpromazine Hydrochloride
Generic name (nonproprietary)
chlorpromazine hydrochloride
Active ingredients
Chlorpromazine hydrochloride — 25 mg/mL
Dosage form
Injection
Route
Intramuscular
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217275
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 70710-1850_97106093-2f0a-4cc9-b580-942b015c6c5bSPL ID 97106093-2f0a-4cc9-b580-942b015c6c5bSPL set ID 7cd6dc0d-e98d-40ae-80d4-c15f63056abfRxCUI 1730076, 1730078UNII 9WP59609J6
Pharmacologic class
Phenothiazine

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N470710185007 followed by a unit qualifier and the quantity

Package 70710-1850-07. 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)

INDICATIONS AND USAGE For the treatment of schizophrenia; to control nausea and vomiting; for relief of restlessness and apprehension before surgery; for acute intermittent porphyria; as an adjunct in the treatment of tetanus; to control the manifestations of the manic type of manic-depressive illness; for relief of intractable hiccups; for the treatment of severe behavioral problems in children (1 year to 12 years of age) marked by combativeness and/or explosive hyperexcitable behavior (out of proportion to immediate provocations), and in the short-term treatment of hyperactive children who show excessive motor activity with accompanying conduct disorders consisting of some or all of the fo…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 217275

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

FDA NDC Directory listings under ANDA 217275
ProductStrengthForm · routeLabelerProduct NDC
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 25 mg/mLInjectionIntramuscularZydus Pharmaceuticals USA Inc.70710-1849
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 25 mg/mLInjectionIntramuscularZydus Lifesciences Limited70771-1778
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 25 mg/mLInjectionIntramuscularZydus Lifesciences Limited70771-1779

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