NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1693Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1693Add 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
71335-1693-1713351693017133516930120 TABLET in 1 BOTTLE (71335-1693-1)Marketed from Oct 13, 2020
71335-1693-2713351693027133516930230 TABLET in 1 BOTTLE (71335-1693-2)Marketed from Dec 10, 2020
71335-1693-3713351693037133516930315 TABLET in 1 BOTTLE (71335-1693-3)Marketed from Dec 29, 2021
71335-1693-4713351693047133516930410 TABLET in 1 BOTTLE (71335-1693-4)Marketed from Sep 3, 2020
71335-1693-5713351693057133516930540 TABLET in 1 BOTTLE (71335-1693-5)Marketed from Dec 29, 2021
71335-1693-6713351693067133516930660 TABLET in 1 BOTTLE (71335-1693-6)Marketed from Dec 29, 2021
71335-1693-7713351693077133516930790 TABLET in 1 BOTTLE (71335-1693-7)Marketed from Dec 29, 2021

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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

Generic name (nonproprietary)
diphenoxylate hydrochloride and atropine sulfate
Active ingredients
Diphenoxylate hydrochloride — 2.5 mg/1Atropine sulfate — .025 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213413
Marketing start
Listing expires
DEA schedule
CV
Other FDA classes
Cholinergic Antagonists (Mechanism)Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 71335-1693_30c2b613-bd3c-46d0-b344-cf46d7a9c616SPL ID 30c2b613-bd3c-46d0-b344-cf46d7a9c616SPL set ID b3f58de9-1cc8-4bc5-842f-010cc48d3582RxCUI 1190572UNII W24OD7YW48, 03J5ZE7KA5
Pharmacologic class
Anticholinergic; Antidiarrheal; Cholinergic Muscarinic 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

N471335169301 followed by a unit qualifier and the quantity

Package 71335-1693-01. 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)

INDICATIONS AND USAGE Diphenoxylate hydrochloride and atropine sulfate tablets are indicated as adjunctive therapy in the management of diarrhea in patients 13 years of age and older.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1693

What is NDC 71335-1693?
71335-1693 is the product NDC for Diphenoxylate Hydrochloride and Atropine Sulfate, Diphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Diphenoxylate Hydrochloride and Atropine Sulfate.
What is the active ingredient?
Diphenoxylate hydrochloride, Atropine sulfate.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Diphenoxylate Hydrochloride and Atropine Sulfate?
26 other product NDCs are listed under this name. See all Diphenoxylate Hydrochloride and Atropine Sulfate 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 Diphenoxylate Hydrochloride and Atropine Sulfate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralAmerican Health Packaging60687-89060687-0890-01
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralREMEDYREPACK INC.70518-391570518-3915-01
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralWinder Laboratories LLC75826-10775826-0107-0075826-0107-0375826-0107-11+2 more
Diphenoxylate Hydrochloride And Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralDirect Rx72189-33672189-0336-1072189-0336-30
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-809068788-8090-02
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-71471610-0714-3071610-0714-5371610-0714-60+3 more
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralSpecGx LLC0406-123600406-1236-0100406-1236-10
Diphenoxylate hydrochloride and atropine sulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralChartwell RX, LLC62135-61862135-0618-12
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralRedpharm Drug67296-224067296-2240-05
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralRedpharm Drug Inc.67296-148567296-1485-09

All 27 Diphenoxylate Hydrochloride and Atropine Sulfate NDCs

Other NDCs under ANDA 213413

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

FDA NDC Directory listings under ANDA 213413
ProductStrengthForm · routeLabelerProduct NDC
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralA-S Medication Solutions50090-5589
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralA-S Medication Solutions50090-5592
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralRedpharm Drug Inc.67296-1485
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralRedpharm Drug67296-2240
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8090
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralLeading Pharma, LLC69315-910
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralREMEDYREPACK INC.70518-3915
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralProficient Rx LP71205-909
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-809
Diphenoxylate Hydrochloride And Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralDirect Rx72189-336
Diphenoxylate Hydrochloride and Atropine SulfateDiphenoxylate hydrochloride 2.5 mg/1; Atropine sulfate .025 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-375

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