Over-the-counter drug · ANDA
Ranitidine NDC 55111-404
Ranitidine hydrochloride 150 mg/1 · Tablet, Coated · Oral · Dr. Reddy's Laboratories Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 55111-404-02 | 55111040402 | 1 BOTTLE in 1 CARTON (55111-404-02) / 200 TABLET, COATED in 1 BOTTLEMarketed from Dec 2, 2009 | |
| 55111-404-17 | 55111040417 | 1 BLISTER PACK in 1 CARTON (55111-404-17) / 8 TABLET, COATED in 1 BLISTER PACKMarketed from Dec 2, 2009 | |
| 55111-404-24 | 55111040424 | 3 BLISTER PACK in 1 CARTON (55111-404-24) / 8 TABLET, COATED in 1 BLISTER PACKMarketed from Dec 2, 2009 | |
| 55111-404-32 | 55111040432 | 1 BOTTLE in 1 CARTON (55111-404-32) / 32 TABLET, COATED in 1 BOTTLEMarketed from Dec 2, 2009 | |
| 55111-404-34 | 55111040434 | 1 BOTTLE in 1 CARTON (55111-404-34) / 24 TABLET, COATED in 1 BOTTLEMarketed from Dec 2, 2009 | |
| 55111-404-36 | 55111040436 | 1 BOTTLE in 1 CARTON (55111-404-36) / 36 TABLET, COATED in 1 BOTTLEMarketed from Dec 2, 2009 | |
| 55111-404-38 | 55111040438 | 4 BLISTER PACK in 1 CARTON (55111-404-38) / 8 TABLET, COATED in 1 BLISTER PACKMarketed from Dec 2, 2009 | |
| 55111-404-40 | 55111040440 | 1 BOTTLE in 1 BOTTLE (55111-404-40) / 40 TABLET, COATED in 1 BOTTLEMarketed from Dec 2, 2009 | |
| 55111-404-50 | 55111040450 | 1 BOTTLE in 1 CARTON (55111-404-50) / 50 TABLET, COATED in 1 BOTTLEMarketed from Dec 2, 2009 | |
| 55111-404-55 | 55111040455 | 2 BOTTLE in 1 CARTON (55111-404-55) / 65 TABLET, COATED in 1 BOTTLEMarketed from Jan 5, 2010 | |
| 55111-404-61 | 55111040461 | 1 BOTTLE in 1 CARTON (55111-404-61) / 65 TABLET, COATED in 1 BOTTLEMarketed from Dec 2, 2009 | |
| 55111-404-62 | 55111040462 | 1 BOTTLE in 1 CARTON (55111-404-62) / 95 TABLET, COATED in 1 BOTTLEMarketed from Dec 2, 2009 | |
| 55111-404-65 | 55111040465 | 1 BOTTLE in 1 CARTON (55111-404-65) / 220 TABLET, COATED in 1 BOTTLEMarketed from Dec 2, 2009 | |
| 55111-404-90 | 55111040490 | 2 BOTTLE in 1 CARTON (55111-404-90) / 95 TABLET, COATED in 1 BOTTLEMarketed from Dec 2, 2009 |
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, Coated
- Route
- Oral
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 078192
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 55111-404_c47f1d10-c4d9-5df4-84e8-55956b47568bSPL ID c47f1d10-c4d9-5df4-84e8-55956b47568bSPL set ID 00df8a42-296f-80dd-98af-ee8b30eb38ccRxCUI 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
N455111040402followed by a unit qualifier and the quantityPackage 55111-0404-02. 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)
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.