Prescription drug · ANDA

Chlorpromazine hydrochloride NDC 70771-1509

Chlorpromazine hydrochloride 100 mg/1 · Tablet, Film coated · Oral · Zydus Lifesciences Limited

NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1509Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1509Add 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
70771-1509-170771150901100 TABLET, FILM COATED in 1 BOTTLE (70771-1509-1)Marketed from Jan 27, 2020 · Sample package
70771-1509-47077115090410 BLISTER PACK in 1 CARTON (70771-1509-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1509-2)Marketed from Jan 27, 2020 · Sample package

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 — 100 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213368
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 70771-1509_bea6994f-8f72-4c2d-8ba3-c74b10f8412dSPL ID bea6994f-8f72-4c2d-8ba3-c74b10f8412dSPL set ID 0ea5e0c6-0062-4be3-96f2-62397da3e77dRxCUI 991039, 991044, 991188, 991194, 991336UNII 9WP59609J6UPC 0370771150618, 0370771150816, 0370771151011, 0370771150915
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 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

N470771150901 followed by a unit qualifier and the quantity

Package 70771-1509-01. 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 .

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 213368

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

FDA NDC Directory listings under ANDA 213368
ProductStrengthForm · routeLabelerProduct NDC
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 50 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1508
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 10 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1506
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 25 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1507
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 200 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1510
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 10 mg/1Tablet, Film coatedOralNorthstar Rx LLC16714-047
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 100 mg/1Tablet, Film coatedOralNorthstar Rx LLC16714-050
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 50 mg/1Tablet, Film coatedOralZydus Pharmaceuticals (USA) Inc.70710-1131
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 10 mg/1Tablet, Film coatedOralZydus Pharmaceuticals (USA) Inc.70710-1129
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 25 mg/1Tablet, Film coatedOralZydus Pharmaceuticals (USA) Inc.70710-1130
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 100 mg/1Tablet, Film coatedOralZydus Pharmaceuticals (USA) Inc.70710-1132
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 200 mg/1Tablet, Film coatedOralZydus Pharmaceuticals (USA) Inc.70710-1133

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Chlorpromazine hydrochloride NDC 70771-1509 | Med-Code