What is NDC 0121-1099?

0121-1099 is the product NDC for calcium chloride, Calcium chloride 100 mg/mL injection, solution, listed with the FDA by PAI Holdings, LLC dba PAI Pharma. It has 1 package NDC, shown above in 10- and 11-digit form.

PAI Holdings, LLC dba PAI Pharma, NDC labeler code 0121. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for calcium chloride?

20 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

calcium chloride NDC 0121-1099 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0121-1099Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00121-1099Add 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	Copy
0121-1099-02	0012110990200121109902	10 VIAL in 1 CARTON (0121-1099-02) / 10 mL in 1 VIAL (0121-1099-55)Marketed from Oct 12, 2026

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): calcium chloride
Generic name (nonproprietary): calcium chloride
Active ingredients: Calcium chloride — 100 mg/mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: PAI Holdings, LLC dba PAI PharmaNDC labeler code 0121
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217463
Marketing start: Oct 12, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 0121-1099_917fd418-9deb-481b-bc64-803a2d28a865SPL ID 917fd418-9deb-481b-bc64-803a2d28a865
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N400121109902 followed by a unit qualifier and the quantity

Package 00121-1099-02. 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

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

About NDC 0121-1099

What is NDC 0121-1099?: 0121-1099 is the product NDC for calcium chloride, Calcium chloride 100 mg/mL injection, solution, listed with the FDA by PAI Holdings, LLC dba PAI Pharma. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: calcium chloride.
What is the active ingredient?: Calcium chloride.
Who is the labeler?: PAI Holdings, LLC dba PAI Pharma, NDC labeler code 0121. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for calcium chloride?: 20 other product NDCs are listed under this name. See all calcium chloride 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 calcium chloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
calcium chloride	Calcium chloride 100 mg/mL	Injection, SolutionIntravenous	Eskayef Pharmaceuticals Limited	72658-1879	72658-1879-02
Calcium Chloridecalcium chloride injection	Calcium chloride 100 mg/mL	Injection, SolutionIntravenous	REMEDYREPACK INC.	70518-4734	70518-4734-00
calcium chloride	Calcium chloride 100 mg/mL	Injection, SolutionIntravenous	SQUARE PHARMACEUTICALS PLC.	76483-108	76483-0108-02
Calcium Chloride	Calcium chloride 100 mg/mL	Injection, SolutionIntravenous	Dr. Reddy's Laboratories Inc.	75907-223	75907-0223-10
Calcium Chloride	Calcium chloride 100 mg/mL	InjectionIntravenous, Intraventricular	REMEDYREPACK INC.	70518-4180	70518-4180-00
calcium chloride	Calcium chloride 100 mg/mL	Injection, SolutionIntravenous	Amneal Pharmaceuticals LLC	70121-2308	70121-2308-04
calcium chloride	Calcium chloride 100 mg/mL	Injection, SolutionIntravenous	Amneal Pharmaceuticals LLC	70121-2309	70121-2309-07
Calcium Chloride	Calcium chloride 100 mg/mL	Injection, SolutionIntravenous	Henry Schein, Inc.	0404-9830	00404-9830-10
Calcium Chloride	Calcium chloride 100 mg/mL	Injection, SolutionIntravenous	Civica, Inc.	72572-052	72572-0052-10
Calcium Chloride	Calcium chloride 100 mg/mL	Injection, SolutionIntravenous	HF Acquisition Co LLC, DBA HealthFirst	51662-1452	51662-1452-01

All 21 calcium chloride NDCs

Other NDCs under ANDA 217463

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

FDA NDC Directory listings under ANDA 217463
Product	Strength	Form · route	Labeler	Product NDC
calcium chloride	Calcium chloride 100 mg/mL	Injection, SolutionIntravenous	Eskayef Pharmaceuticals Limited	72658-1879
calcium chloride	Calcium chloride 100 mg/mL	Injection, SolutionIntravenous	SQUARE PHARMACEUTICALS PLC.	76483-108