Equate Cimetidine (cimetidine) NDC 49035-820

NDC codes

FDA NDC Directory

Product NDC (as listed)49035-820Labeler and product segments. Claims need a package NDC.

Product NDC at billing width49035-0820Add 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
49035-820-72	49035082072	1 BOTTLE in 1 CARTON (49035-820-72) / 60 TABLET, FILM COATED in 1 BOTTLEMarketed from Sep 27, 2006
49035-820-76	49035082076	1 BOTTLE in 1 CARTON (49035-820-76) / 120 TABLET, FILM COATED in 1 BOTTLEMarketed from May 31, 2021

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): Equate Cimetidine
Generic name (nonproprietary): cimetidine
Active ingredients: Cimetidine — 200 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Wal-Mart Stores Inc
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075285
Marketing start: Sep 27, 2006
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 49035-820_4c4930d7-ec4b-45eb-8706-d06523a0d198SPL ID 4c4930d7-ec4b-45eb-8706-d06523a0d198SPL set ID ad3e8f6a-8e35-42c2-a98c-566a2868e923RxCUI 197505UNII 80061L1WGD
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

N449035082072 followed by a unit qualifier and the quantity

Package 49035-0820-72. 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 Mar 10, 2022.

Indications (excerpt from the label)

Uses • relieves heartburn associated with acid indigestion and sour stomach • prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain food and beverages

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 075285

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

FDA NDC Directory listings under ANDA 075285
Product	Strength	Form · route	Labeler	Product NDC
cimetidine 200 acid reducercimetidine	Cimetidine 200 mg/1	Tablet, Film coatedOral	Walgreen Company	0363-0022
Acid Controllercimetidine	Cimetidine 200 mg/1	Tablet, Film coatedOral	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	51316-739
heartburn preventioncimetidine	Cimetidine 200 mg/1	Tablet, Film coatedOral	H E B	59640-022
basic care acid reducercimetidine	Cimetidine 200 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-022
Acid Reducercimetidine	Cimetidine 200 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-470
heartburn reliefcimetidine	Cimetidine 200 mg/1	Tablet, Film coatedOral	CVS Pharmacy	59779-022