Over-the-counter drug · ANDA
Ranitidine NDC 55111-131
Ranitidine hydrochloride 75 mg/1 · Tablet · Oral · Dr. Reddy's Laboratories Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 55111-131-04 | 5511101310455111013104 | 1 BOTTLE in 1 CARTON (55111-131-04) / 120 TABLET in 1 BOTTLEMarketed from Mar 1, 2000 | |
| 55111-131-14 | 5511101311455111013114 | 2 BLISTER PACK in 1 CARTON (55111-131-14) / 10 TABLET in 1 BLISTER PACKMarketed from Mar 1, 2000 | |
| 55111-131-30 | 5511101313055111013130 | 1 BOTTLE in 1 CARTON (55111-131-30) / 30 TABLET in 1 BOTTLEMarketed from Mar 1, 2000 | |
| 55111-131-37 | 5511101313755111013137 | 1 BOTTLE in 1 CARTON (55111-131-37) / 160 TABLET in 1 BOTTLEMarketed from Mar 1, 2000 | |
| 55111-131-45 | 5511101314555111013145 | 1 BOTTLE in 1 CARTON (55111-131-45) / 45 TABLET in 1 BOTTLEMarketed from Mar 1, 2000 | |
| 55111-131-60 | 5511101316055111013160 | 1 BOTTLE in 1 CARTON (55111-131-60) / 60 TABLET in 1 BOTTLEMarketed from Mar 1, 2000 | |
| 55111-131-79 | 5511101317955111013179 | 1 BLISTER PACK in 1 CARTON (55111-131-79) / 10 TABLET in 1 BLISTER PACKMarketed from Mar 1, 2000 | |
| 55111-131-80 | 5511101318055111013180 | 1 BOTTLE in 1 CARTON (55111-131-80) / 80 TABLET in 1 BOTTLEMarketed from Mar 1, 2000 | |
| 55111-131-81 | 5511101318155111013181 | 3 BLISTER PACK in 1 CARTON (55111-131-81) / 10 TABLET in 1 BLISTER PACKMarketed from Mar 1, 2000 | |
| 55111-131-90 | 5511101319055111013190 | 1 BOTTLE in 1 CARTON (55111-131-90) / 90 TABLET in 1 BOTTLEMarketed from Mar 1, 2000 |
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 — 75 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Dr. Reddy's Laboratories LimitedNDC labeler code 55111
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 075294
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 55111-131_210e3c0b-be93-aa50-550d-e383e7d5f19eSPL ID 210e3c0b-be93-aa50-550d-e383e7d5f19eSPL set ID 12a38e29-130c-6d41-1753-acccb0b41efeRxCUI 312773UNII 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
N455111013104followed by a unit qualifier and the quantityPackage 55111-0131-04. 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)
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.
About NDC 55111-131
- What is NDC 55111-131?
- 55111-131 is the product NDC for Ranitidine, Ranitidine hydrochloride 75 mg/1 tablet, listed with the FDA by Dr. Reddy's Laboratories Limited. It has 10 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Ranitidine.
- What is the active ingredient?
- Ranitidine hydrochloride.
- Who is the labeler?
- Dr. Reddy's Laboratories Limited, NDC labeler code 55111. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Ranitidine?
- 12 other product NDCs are listed under this name. See all Ranitidine NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Ranitidine products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Ranitidine | Ranitidine hydrochloride 150 mg/1 | TabletOral | Atland Pharmaceuticals, LLC | 71993-314 | 71993-0314-30 |
| Ranitidine | Ranitidine hydrochloride 300 mg/1 | TabletOral | Atland Pharmaceuticals, LLC | 71993-315 | 71993-0315-30 |
| Ranitidine | Ranitidine hydrochloride 150 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 64980-636 | 64980-0636-03 |
| Ranitidine | Ranitidine hydrochloride 300 mg/1 | TabletOral | Rising Pharma Holdings, Inc. | 64980-637 | 64980-0637-03 |
| Ranitidine | Ranitidine hydrochloride 150 mg/1 | TabletOral | Granules India Ltd | 62207-773 | 62207-0773-3662207-0773-4162207-0773-47+1 more |
| Ranitidine | Ranitidine hydrochloride 150 mg/1 | CapsuleOral | Ajanta Pharma USA Inc. | 27241-109 | 27241-0109-0627241-0109-50 |
| Ranitidine | Ranitidine hydrochloride 300 mg/1 | CapsuleOral | Ajanta Pharma USA Inc. | 27241-110 | 27241-0110-0327241-0110-10 |
| Ranitidine | Ranitidine 15 mg/mL | SyrupOral | Pharmaceutical Associates, Inc. | 0121-0727 | 00121-0727-16 |
| Ranitidine | Ranitidine 15 mg/mL | SyrupOral | Pharmaceutical Associates, Inc. | 0121-4727 | 00121-4727-10 |
| Ranitidine | Ranitidine hydrochloride 150 mg/1 | TabletOral | Amneal Pharmaceuticals of New York LLC | 53746-253 | 53746-0253-0153746-0253-0553746-0253-10+2 more |