Prescription drug · ANDA

Chlorpromazine hydrochloride NDC 70771-1507

Chlorpromazine hydrochloride 25 mg/1 · Tablet, Film coated · Oral · Zydus Lifesciences Limited

NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1507Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1507Add 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
70771-1507-17077115070170771150701100 TABLET, FILM COATED in 1 BOTTLE (70771-1507-1)Marketed from Jan 27, 2020 · Sample package
70771-1507-4707711507047077115070410 BLISTER PACK in 1 CARTON (70771-1507-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1507-2)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 — 25 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Zydus Lifesciences LimitedNDC labeler code 70771
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 70771-1507_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

N470771150701 followed by a unit qualifier and the quantity

Package 70771-1507-01. 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)

About NDC 70771-1507

What is NDC 70771-1507?
70771-1507 is the product NDC for Chlorpromazine hydrochloride, Chlorpromazine hydrochloride 25 mg/1 tablet, film coated, listed with the FDA by Zydus Lifesciences Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Chlorpromazine hydrochloride.
What is the active ingredient?
Chlorpromazine hydrochloride.
Who is the labeler?
Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Chlorpromazine hydrochloride?
106 other product NDCs are listed under this name. See all Chlorpromazine hydrochloride 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 Chlorpromazine hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 25 mg/1Tablet, Sugar coatedOralAmerican Health Packaging60687-93860687-0938-0160687-0938-65
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 50 mg/1Tablet, Sugar coatedOralAmerican Health Packaging60687-94960687-0949-01
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 100 mg/1Tablet, Sugar coatedOralAmerican Health Packaging60687-96060687-0960-01
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 200 mg/1Tablet, Sugar coatedOralAmerican Health Packaging60687-97160687-0971-01
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 100 mg/mLConcentrateOralSaptalis Pharmaceuticals, LLC.71656-10171656-0101-08
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 30 mg/mLConcentrateOralSaptalis Pharmaceuticals, LLC.71656-10271656-0102-04
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 25 mg/mLInjectionIntramuscularNovadoz Pharmaceuticals LLC72205-19072205-0190-25
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 25 mg/mLInjectionIntramuscularNovadoz Pharmaceuticals LLC72205-19172205-0191-25
Chlorpromazine HydrochlorideChlorpromazine hydrochloride 25 mg/1Tablet, Sugar coatedOralCoupler LLC67046-163367046-1633-03
chlorpromazine hydrochlorideChlorpromazine hydrochloride 30 mg/mLConcentrateOralAdvagen Pharma Ltd72888-45772888-0457-01

All 107 Chlorpromazine hydrochloride NDCs

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 10 mg/1Tablet, Film coatedOralNorthstar Rx LLC16714-047
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 100 mg/1Tablet, Film coatedOralNorthstar Rx LLC16714-050
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 50 mg/1Tablet, Film coatedOralZydus Pharmaceuticals (USA) Inc.70710-1131
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
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 10 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1506
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 50 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1508
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 100 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1509
Chlorpromazine hydrochlorideChlorpromazine hydrochloride 200 mg/1Tablet, Film coatedOralZydus Lifesciences Limited70771-1510

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