NDC codes

FDA NDC Directory
Product NDC (as listed)63187-333Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63187-0333Add 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
63187-333-30631870333306318703333030 TABLET, FILM COATED in 1 BOTTLE (63187-333-30)Marketed from Jan 1, 2019

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)
Cimetidine
Generic name (nonproprietary)
cimetidine
Active ingredients
Cimetidine — 400 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 63187
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074151
Marketing start
Listing expires
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 63187-333_6996efbc-1bc5-48b5-a3d3-38a3595d5f5bSPL ID 6996efbc-1bc5-48b5-a3d3-38a3595d5f5bSPL set ID 5c2e1f52-4021-4f70-9b2b-63af17094187RxCUI 197507UNII 80061L1WGDUPC 0363187333300

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

N463187033330 followed by a unit qualifier and the quantity

Package 63187-0333-30. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Cimetidine tablets are indicated in: • Short-term treatment of active duodenal ulcer. Most patients heal within 4 weeks and there is rarely reason to use cimetidine at full dosage for longer than 6 to 8 weeks (see DOSAGE AND ADMINISTRATION , Duodenal Ulcer ). Concomitant antacids should be given as needed for relief of pain. However, simultaneous administration of oral cimetidine and antacids is not recommended, since antacids have been reported to interfere with the absorption of oral cimetidine. • Maintenance therapy for duodenal ulcer patients at reduced dosage after healing of active ulcer. Patients have been maintained on continued treatment with cimetidine 400 mg …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63187-333

What is NDC 63187-333?
63187-333 is the product NDC for Cimetidine, Cimetidine 400 mg/1 tablet, film coated, listed with the FDA by Proficient Rx LP. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Cimetidine.
What is the active ingredient?
Cimetidine.
Who is the labeler?
Proficient Rx LP, NDC labeler code 63187. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cimetidine?
21 other product NDCs are listed under this name. See all Cimetidine 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 Cimetidine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
CimetidineCimetidine 200 mg/1Tablet, Film coatedOralBionpharma Inc.69452-32369452-0323-2069452-0323-30
CimetidineCimetidine 300 mg/1Tablet, Film coatedOralBionpharma Inc.69452-32469452-0324-2069452-0324-30
CimetidineCimetidine 400 mg/1Tablet, Film coatedOralBionpharma Inc.69452-32569452-0325-2069452-0325-30
CimetidineCimetidine 800 mg/1Tablet, Film coatedOralBionpharma Inc.69452-32669452-0326-2069452-0326-30
CimetidineCimetidine 400 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-82559651-0825-0159651-0825-05
CimetidineCimetidine 800 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-82659651-0826-01
CimetidineCimetidine 400 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-69751655-0697-51
CimetidineCimetidine 400 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-050050090-0500-0050090-0500-01
CimetidineCimetidine 800 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-830500093-8305-01
CimetidineCimetidine 300 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-819200093-8192-0100093-8192-05

All 22 Cimetidine NDCs

Other NDCs under ANDA 074151

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

FDA NDC Directory listings under ANDA 074151
ProductStrengthForm · routeLabelerProduct NDC
CimetidineCimetidine 300 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-8192
CimetidineCimetidine 400 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-0500
CimetidineCimetidine 300 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-1783

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