Over-the-counter drug · OTC MONOGRAPH DRUG
Stimulant Laxative Enteric Coated (Bisacodyl) NDC 66424-002
Bisacodyl 5 mg/1 · Tablet · Oral · SDA Laboratories, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 66424-002-01 | 6642400020166424000201 | 100 TABLET in 1 BOTTLE (66424-002-01)Marketed from Jul 1, 2025 |
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)
- Stimulant Laxative Enteric Coated
- Generic name (nonproprietary)
- bisacodyl
- Active ingredients
- Bisacodyl — 5 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- SDA Laboratories, Inc.NDC labeler code 66424
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Other FDA classes
- Increased Large Intestinal Motility (Physiologic effect)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
- Identifiers
- Product ID 66424-002_353f5482-02fd-f0ab-e063-6294a90a88acSPL ID 353f5482-02fd-f0ab-e063-6294a90a88acSPL set ID 017bc27d-a951-48a4-8f65-90fcbe6dbea0RxCUI 308753UNII 10X0709Y6IUPC 0646425000081
- Pharmacologic class
- Stimulant Laxative
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
N466424000201followed by a unit qualifier and the quantityPackage 66424-0002-01. 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 for relief of occasional constipation and irregularity this product generally produces bowel movement in 6 to 12 hours
Excerpt only. Read the full label for complete information.
About NDC 66424-002
- What is NDC 66424-002?
- 66424-002 is the product NDC for Stimulant Laxative Enteric Coated, Bisacodyl 5 mg/1 tablet, listed with the FDA by SDA Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Stimulant Laxative Enteric Coated (Bisacodyl).
- What is the active ingredient?
- Bisacodyl.
- Who is the labeler?
- SDA Laboratories, Inc., NDC labeler code 66424. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Stimulant Laxative Enteric Coated?
- 4 other product NDCs are listed under this name. See all Stimulant Laxative Enteric Coated NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Stimulant Laxative Enteric Coated products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| stimulant laxative enteric coatedbisacodyl | Bisacodyl 5 mg/1 | TabletOral | Sportpharm LLC | 85766-148 | 85766-0148-0085766-0148-0185766-0148-02+2 more |
| stimulant laxative enteric coatedbisacodyl | Bisacodyl 5 mg/1 | TabletOral | Geri-Care Pharmaceutical Corp | 57896-441 | 57896-0441-0157896-0441-1057896-0441-20+2 more |
| stimulant laxative enteric coatedbisacodyl | Bisacodyl 5 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-1531 | 71335-1531-0071335-1531-0171335-1531-02+7 more |
| stimulant laxative enteric coatedbisacodyl | Bisacodyl 5 mg/1 | TabletOral | Aphena Pharma Solutions - Tennessee, LLC | 71610-453 | 71610-0453-0271610-0453-0471610-0453-20 |
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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