NDC codes

FDA NDC Directory
Product NDC (as listed)0093-8305Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00093-8305Add 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 NDC11-digit (billing)PackageCopy
0093-8305-010009383050100093830501100 TABLET, FILM COATED in 1 BOTTLE (0093-8305-01)Marketed from Dec 23, 2003

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
Generic name (nonproprietary)
cimetidine
Active ingredients
Cimetidine — 800 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Teva Pharmaceuticals USA, Inc.NDC labeler code 0093
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 074463
Marketing start
Listing expires
Other FDA classes
Histamine H2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 0093-8305_629411bd-d0df-467e-bab1-4fef95f9e46fSPL ID 629411bd-d0df-467e-bab1-4fef95f9e46f

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

N400093830501 followed by a unit qualifier and the quantity

Package 00093-8305-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 0093-8305

What is NDC 0093-8305?
0093-8305 is the product NDC for Cimetidine, Cimetidine 800 mg/1 tablet, film coated, listed with the FDA by Teva Pharmaceuticals USA, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Cimetidine.
What is the active ingredient?
Cimetidine.
Who is the labeler?
Teva Pharmaceuticals USA, Inc., NDC labeler code 0093. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cimetidine?
21 other product NDCs are listed under this name. See all Cimetidine NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Cimetidine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
CimetidineCimetidine 200 mg/1Tablet, Film coatedOralBionpharma Inc.69452-32369452-0323-2069452-0323-30
CimetidineCimetidine 300 mg/1Tablet, Film coatedOralBionpharma Inc.69452-32469452-0324-2069452-0324-30
CimetidineCimetidine 400 mg/1Tablet, Film coatedOralBionpharma Inc.69452-32569452-0325-2069452-0325-30
CimetidineCimetidine 800 mg/1Tablet, Film coatedOralBionpharma Inc.69452-32669452-0326-2069452-0326-30
CimetidineCimetidine 400 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-82559651-0825-0159651-0825-05
CimetidineCimetidine 800 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-82659651-0826-01
CimetidineCimetidine 400 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-69751655-0697-51
CimetidineCimetidine 400 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-050050090-0500-0050090-0500-01
CimetidineCimetidine 400 mg/1Tablet, Film coatedOralProficient Rx LP63187-33363187-0333-30
CimetidineCimetidine 300 mg/1Tablet, Film coatedOralTeva Pharmaceuticals USA, Inc.0093-819200093-8192-0100093-8192-05

All 22 Cimetidine NDCs

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