ChlorproMAZINE Hydrochloride - ChlorproMAZINE 25 mg / 1 Tablet 1000 Tablet, Sugar Coated

Reference details for licensed healthcare facility review and verification.

NDC 1163304-0143-10
Product NDC63304-0143
Generic Drug NameChlorproMAZINE
Brand NameChlorproMAZINE Hydrochloride
ManufacturerSun Pharmaceutical Industries Inc
Strength25 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity1000 Tablet, Sugar Coated
Package Description1000 TABLET, SUGAR COATED in 1 BOTTLE (63304-143-10)
Active IngredientsChlorpromazine Hydrochloride
Marketing CategoryANDA

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NDC snapshot

ChlorproMAZINE 25 mg / 1 Tablet is tracked under NDC 63304-0143-10 and rolls up into product family 63304-0143. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 1000 Tablet, Sugar Coated.
  • Manufacturer: Sun Pharmaceutical Industries Inc.
  • Dosage form: Tablet.
  • Family size: 2 indexed presentations.

Official references

Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.

Alternate presentations in this family

These nearby package-level pages can help healthcare teams compare related packaging or presentation differences inside the same product-NDC family.

ChlorproMAZINE Hydrochloride - ChlorproMAZINE 25 mg / 1 Tablet 1000 Tablet, Sugar Coated, NDC 63304-0143-10, is a Sun Pharmaceutical Industries Inc 25 mg / 1 tablet presentation packaged as 1000 Tablet, Sugar Coated.

NDC search formats

  • Canonical NDC 11: 63304-0143-10
  • Digits-only NDC 11: 63304014310
  • Possible 10-digit display format: 63304-143-10 (6330414310)

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