Ranitidine NDC 62207-773

NDC codes

FDA NDC Directory

Product NDC (as listed)62207-773Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62207-0773Add 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
62207-773-36	62207077336	5 BAG in 1 CARTON (62207-773-36) / 10000 TABLET in 1 BAG (62207-773-32)Marketed from Jun 26, 2019
62207-773-41	62207077341	1 BOTTLE in 1 CARTON (62207-773-41) / 24 TABLET in 1 BOTTLEMarketed from Jun 26, 2019
62207-773-47	62207077347	1 BOTTLE in 1 CARTON (62207-773-47) / 500 TABLET in 1 BOTTLEMarketed from Jun 26, 2019
62207-773-58	62207077358	2 BLISTER PACK in 1 CARTON (62207-773-58) / 10 TABLET in 1 BLISTER PACKMarketed from Jun 26, 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): Ranitidine
Generic name (nonproprietary): ranitidine
Active ingredients: Ranitidine hydrochloride — 150 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Granules India Ltd
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210243
Marketing start: Jun 26, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 62207-773_44f2b222-ae43-eef4-e063-6394a90ab2b6SPL ID 44f2b222-ae43-eef4-e063-6394a90ab2b6SPL set ID aab81d9f-397d-49fb-8083-77a1872cc71fRxCUI 198191UNII BK76465IHM
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

N462207077336 followed by a unit qualifier and the quantity

Package 62207-0773-36. 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 Dec 2, 2025.

Indications (excerpt from the label)

USE(S) ◾ 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 210243

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

FDA NDC Directory listings under ANDA 210243
Product	Strength	Form · route	Labeler	Product NDC
Ranitidine cool mintranitidine	Ranitidine hydrochloride 150 mg/1	TabletOral	Granules India Ltd	62207-774