Over-the-counter drug · NDA
Tagamet (cimetidine) NDC 63029-222
Cimetidine 200 mg/1 · Tablet · Oral · Medtech Products Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 63029-222-01 | 63029022201 | 1 BLISTER PACK in 1 BOX (63029-222-01) / 30 TABLET in 1 BLISTER PACKMarketed from Jun 1, 2012 | |
| 63029-222-02 | 63029022202 | 1 BLISTER PACK in 1 BOX (63029-222-02) / 6 TABLET in 1 BLISTER PACKMarketed from Jun 1, 2012 | |
| 63029-222-03 | 63029022203 | 1 BLISTER PACK in 1 BOX (63029-222-03) / 50 TABLET in 1 BLISTER PACKMarketed from Jun 1, 2012 | |
| 63029-222-04 | 63029022204 | 4 BLISTER PACK in 1 BOX (63029-222-04) / 10 TABLET in 1 BLISTER PACKMarketed from Jun 1, 2019 | |
| 63029-222-05 | 63029022205 | 4 BLISTER PACK in 1 BOX (63029-222-05) / 9 TABLET in 1 BLISTER PACKMarketed from Jun 1, 2019 | |
| 63029-222-06 | 63029022206 | 7 BLISTER PACK in 1 BOX (63029-222-06) / 10 TABLET in 1 BLISTER PACKMarketed from Jun 1, 2012 | |
| 63029-222-09 | 63029022209 | 1 BOTTLE in 1 CARTON (63029-222-09) / 90 TABLET in 1 BOTTLEMarketed from Jun 1, 2012 | |
| 63029-222-11 | 63029022211 | 1 BOTTLE in 1 CARTON (63029-222-11) / 100 TABLET in 1 BOTTLEMarketed from Jun 1, 2012 | |
| 63029-222-12 | 63029022212 | 2 BLISTER PACK in 1 BOX (63029-222-12) / 6 TABLET in 1 BLISTER PACKMarketed from Jun 1, 2012 | |
| 63029-222-70 | 63029022270 | 1 BOTTLE in 1 CARTON (63029-222-70) / 70 TABLET in 1 BOTTLEMarketed from Jun 1, 2012 |
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)
- Tagamet
- Generic name (nonproprietary)
- cimetidine
- Active ingredients
- Cimetidine — 200 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Medtech Products Inc.
- Product type
- Over-the-counter drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 020238
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 63029-222_e29142a4-59e0-4f6d-8a1f-3050b21491a2SPL ID e29142a4-59e0-4f6d-8a1f-3050b21491a2SPL set ID e6401e0a-8612-42e8-bf89-2d67243f28dcRxCUI 104062, 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
N463029022201followed by a unit qualifier and the quantityPackage 63029-0222-01. 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.
Other NDCs under NDA 020238
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.