cimetidine 200 acid reducer (cimetidine) NDC 0363-0022

NDC codes

FDA NDC Directory

Product NDC (as listed)0363-0022Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00363-0022Add 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
0363-0022-72	00363002272	1 BOTTLE in 1 CARTON (0363-0022-72) / 60 TABLET, FILM COATED in 1 BOTTLEMarketed from Apr 14, 2010

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 200 acid reducerSuffix: acid reducer
Generic name (nonproprietary): cimetidine
Active ingredients: Cimetidine — 200 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Walgreen Company
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075285
Marketing start: Mar 27, 2001
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 0363-0022_84970421-ebbc-45ad-a5ca-58038d3bf539SPL ID 84970421-ebbc-45ad-a5ca-58038d3bf539SPL set ID 7087f4bb-992b-4680-a9a7-452ce74eed2dRxCUI 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

N400363002272 followed by a unit qualifier and the quantity

Package 00363-0022-72. 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, 2025.

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 foods 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
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
Equate Cimetidinecimetidine	Cimetidine 200 mg/1	Tablet, Film coatedOral	Wal-Mart Stores Inc	49035-820
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