What is NDC 62135-632?

62135-632 is the product NDC for Cimetidine, Cimetidine 400 mg/1 tablet, film coated, listed with the FDA by Chartwell RX, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Chartwell RX, LLC, NDC labeler code 62135. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Cimetidine NDC 62135-632 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62135-632Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62135-0632Add 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 NDC	11-digit (billing)	Package	Copy
62135-632-90	6213506329062135063290	90 TABLET, FILM COATED in 1 BOTTLE (62135-632-90)Marketed from Aug 15, 2023

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: Chartwell RX, LLCNDC labeler code 62135
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074329
Marketing start: May 17, 1994
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 62135-632_0337689b-c5d5-d881-e063-6394a90aaec9SPL ID 0337689b-c5d5-d881-e063-6394a90aaec9SPL set ID 01997826-7ca1-473e-bfc9-075b14b58a35RxCUI 197505, 197506, 197507, 197508UNII 80061L1WGDUPC 0362135633905, 0362135630300, 0362135631901, 0362135632908
Pharmacologic class: Histamine-2 Receptor Antagonist

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

N462135063290 followed by a unit qualifier and the quantity

Package 62135-0632-90. 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 Aug 18, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE Cimetidine tablets are indicated in: 1. Short-term treatment of active duodenal ulcer. Most patients heal within 4 weeks and there is rarely reason to use cimetidine tablets 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 cimetidine tablets and antacids is not recommended, since antacids have been reported to interfere with the absorption of cimetidine. 2. Maintenance therapy for duodenal ulcer patients at reduced dosage after healing of active ulcer. Patients have been maintained on continued treatment with cimetidine …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62135-632

What is NDC 62135-632?: 62135-632 is the product NDC for Cimetidine, Cimetidine 400 mg/1 tablet, film coated, listed with the FDA by Chartwell RX, LLC. 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?: Chartwell RX, LLC, NDC labeler code 62135. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Cimetidine	Cimetidine 200 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-323	69452-0323-2069452-0323-30
Cimetidine	Cimetidine 300 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-324	69452-0324-2069452-0324-30
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-325	69452-0325-2069452-0325-30
Cimetidine	Cimetidine 800 mg/1	Tablet, Film coatedOral	Bionpharma Inc.	69452-326	69452-0326-2069452-0326-30
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-825	59651-0825-0159651-0825-05
Cimetidine	Cimetidine 800 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-826	59651-0826-01
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-697	51655-0697-51
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-0500	50090-0500-0050090-0500-01
Cimetidine	Cimetidine 400 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-333	63187-0333-30
Cimetidine	Cimetidine 800 mg/1	Tablet, Film coatedOral	Teva Pharmaceuticals USA, Inc.	0093-8305	00093-8305-01

All 22 Cimetidine NDCs

Other NDCs under ANDA 074329

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

FDA NDC Directory listings under ANDA 074329
Product	Strength	Form · route	Labeler	Product NDC
Cimetidine	Cimetidine 200 mg/1	Tablet, Film coatedOral	Chartwell RX, LLC	62135-630
Cimetidine	Cimetidine 300 mg/1	Tablet, Film coatedOral	Chartwell RX, LLC	62135-631
Cimetidine	Cimetidine 800 mg/1	Tablet, Film coatedOral	Chartwell RX, LLC	62135-633