What is NDC 52268-012?

52268-012 is the product NDC for SUPREP Bowel Prep, Sodium sulfate 17.5 g/mL + 2 more ingredients solution, concentrate, listed with the FDA by Braintree Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

SUPREP Bowel Prep (Sodium sulfate, potassium sulfate, magnesium sulfate).

What is the active ingredient?

Sodium sulfate, Potassium sulfate, Magnesium sulfate, Unspecified form.

Braintree Laboratories, Inc., NDC labeler code 52268. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for SUPREP Bowel Prep?

3 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

SUPREP Bowel Prep NDC 52268-012 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)52268-012Labeler and product segments. Claims need a package NDC.

Product NDC at billing width52268-0012Add 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
52268-012-01	5226800120152268001201	2 BOTTLE, PLASTIC in 1 CARTON (52268-012-01) / 177.4 mL in 1 BOTTLE, PLASTICMarketed from Aug 5, 2010

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): SUPREP Bowel Prep
Generic name (nonproprietary): sodium sulfate, potassium sulfate, magnesium sulfate
Active ingredients: Sodium sulfate — 17.5 g/mLPotassium sulfate — 3.13 g/mLMagnesium sulfate, Unspecified form — 1.6 g/mL
Dosage form: Solution, Concentrate
Route: Oral
Labeler: Braintree Laboratories, Inc.NDC labeler code 52268
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 022372
Marketing start: Aug 5, 2010
Marketing end: Jan 31, 2028
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 52268-012_5d537ee4-dc8c-32dd-e063-6294a90a4fbeSPL ID 5d537ee4-dc8c-32dd-e063-6294a90a4fbe
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative; Potassium Salt

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

N452268001201 followed by a unit qualifier and the quantity

Package 52268-0012-01. 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 52268-012

What is NDC 52268-012?: 52268-012 is the product NDC for SUPREP Bowel Prep, Sodium sulfate 17.5 g/mL + 2 more ingredients solution, concentrate, listed with the FDA by Braintree Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: SUPREP Bowel Prep (Sodium sulfate, potassium sulfate, magnesium sulfate).
What is the active ingredient?: Sodium sulfate, Potassium sulfate, Magnesium sulfate, Unspecified form.
Who is the labeler?: Braintree Laboratories, Inc., NDC labeler code 52268. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for SUPREP Bowel Prep?: 3 other product NDCs are listed under this name. See all SUPREP Bowel Prep 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 SUPREP Bowel Prep NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
SUPREP Bowel Prepsodium sulfate, potassium sulfate, magnesium sulfate	Sodium sulfate 17.5 g/mL + 2 more ingredients	Solution, ConcentrateOral	Azurity Pharmaceuticals, Inc.	24338-175	24338-0175-01
SUPREP Bowel Prepsodium sulfate, potassium sulfate, magnesium sulfate	Sodium sulfate 13.13 g/133.1mL + 2 more ingredients	Solution, ConcentrateOral	Azurity Pharmaceuticals, Inc.	24338-177	24338-0177-01
SUPREP Bowel Prepsodium sulfate, potassium sulfate, magnesium sulfate	Sodium sulfate 13.13 g/133.1mL + 2 more ingredients	Solution, ConcentrateOral	Braintree Laboratories, Inc.	52268-112	52268-0112-01

Other NDCs under NDA 022372

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

FDA NDC Directory listings under NDA 022372
Product	Strength	Form · route	Labeler	Product NDC
Sodium Sulfate, Potassium Sulfate And Magnesium Sulfatesodium sulfate, potassium sulfate, magnesium sulfate	Sodium sulfate 17.5 g/mL + 2 more ingredients	Solution, ConcentrateOral	Affordable Pharmaceuticals, LLC	10572-012
Sodium Sulfate, Potassium Sulfate And Magnesium Sulfatesodium sulfate, potassium sulfate, magnesium sulfate	Sodium sulfate 13.13 g/133.1mL + 2 more ingredients	Solution, ConcentrateOral	Affordable Pharmaceuticals, LLC	10572-112
Sodium Sulfate, Potassium Sulfate And Magnesium Sulfatesodium sulfate, potassium sulfate, magnesium sulfate	Sodium sulfate 17.5 g/mL + 2 more ingredients	Solution, ConcentrateOral	Wilshire Pharmaceuticals, Inc.	52536-175
Sodium Sulfate, Potassium Sulfate And Magnesium Sulfatesodium sulfate, potassium sulfate, magnesium sulfate	Sodium sulfate 13.13 g/133.1mL + 2 more ingredients	Solution, ConcentrateOral	Wilshire Pharmaceuticals, Inc.	52536-177
SUPREP Bowel Prepsodium sulfate, potassium sulfate, magnesium sulfate	Sodium sulfate 17.5 g/mL + 2 more ingredients	Solution, ConcentrateOral	Azurity Pharmaceuticals, Inc.	24338-175
SUPREP Bowel Prepsodium sulfate, potassium sulfate, magnesium sulfate	Sodium sulfate 13.13 g/133.1mL + 2 more ingredients	Solution, ConcentrateOral	Azurity Pharmaceuticals, Inc.	24338-177
SUPREP Bowel Prepsodium sulfate, potassium sulfate, magnesium sulfate	Sodium sulfate 13.13 g/133.1mL + 2 more ingredients	Solution, ConcentrateOral	Braintree Laboratories, Inc.	52268-112