What is NDC 71205-936?

71205-936 is the product NDC for Miglitol, Miglitol 50 mg/1 tablet, coated, listed with the FDA by Proficient Rx LP. It has 4 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Miglitol?

5 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Miglitol NDC 71205-936 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-936Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0936Add 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
71205-936-00	71205093600	100 TABLET, COATED in 1 BOTTLE (71205-936-00)Marketed from Mar 1, 2021
71205-936-30	71205093630	30 TABLET, COATED in 1 BOTTLE (71205-936-30)Marketed from Mar 1, 2021
71205-936-60	71205093660	60 TABLET, COATED in 1 BOTTLE (71205-936-60)Marketed from Mar 1, 2021
71205-936-90	71205093690	90 TABLET, COATED in 1 BOTTLE (71205-936-90)Marketed from Mar 1, 2021

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): Miglitol
Generic name (nonproprietary): miglitol
Active ingredients: Miglitol — 50 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203965
Marketing start: Jan 15, 2021
Listing expires: Dec 31, 2026
Other FDA classes: alpha Glucosidase Inhibitors (Mechanism)
Identifiers: Product ID 71205-936_c8003a86-3d92-4acb-b8b8-fe52835c83f5SPL ID c8003a86-3d92-4acb-b8b8-fe52835c83f5SPL set ID f16ecb50-e54e-43e1-8789-eaf5bc94f332RxCUI 205329, 205330, 205331UNII 0V5436JAQWUPC 0371205935306
Pharmacologic class: alpha-Glucosidase Inhibitor

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

N471205093600 followed by a unit qualifier and the quantity

Package 71205-0936-00. 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 Apr 1, 2022.

Indications (excerpt from the label)

INDICATIONS AND USAGE Miglitol tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-936

What is NDC 71205-936?: 71205-936 is the product NDC for Miglitol, Miglitol 50 mg/1 tablet, coated, listed with the FDA by Proficient Rx LP. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Miglitol.
What is the active ingredient?: Miglitol.
Who is the labeler?: Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Miglitol?: 5 other product NDCs are listed under this name. See all Miglitol 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 Miglitol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Miglitol	Miglitol 25 mg/1	Tablet, CoatedOral	Westminster Pharmaceuticals, LLC	69367-303	69367-0303-01
Miglitol	Miglitol 50 mg/1	Tablet, CoatedOral	Westminster Pharmaceuticals, LLC	69367-304	69367-0304-01
Miglitol	Miglitol 100 mg/1	Tablet, CoatedOral	Westminster Pharmaceuticals, LLC	69367-305	69367-0305-01
Miglitol	Miglitol 25 mg/1	Tablet, CoatedOral	Proficient Rx LP	71205-935	71205-0935-0071205-0935-3071205-0935-60+1 more
Miglitol	Miglitol 100 mg/1	Tablet, CoatedOral	Proficient Rx LP	71205-937	71205-0937-0071205-0937-3071205-0937-60+1 more

Other NDCs under ANDA 203965

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

FDA NDC Directory listings under ANDA 203965
Product	Strength	Form · route	Labeler	Product NDC
Miglitol	Miglitol 25 mg/1	Tablet, CoatedOral	Westminster Pharmaceuticals, LLC	69367-303
Miglitol	Miglitol 50 mg/1	Tablet, CoatedOral	Westminster Pharmaceuticals, LLC	69367-304
Miglitol	Miglitol 100 mg/1	Tablet, CoatedOral	Westminster Pharmaceuticals, LLC	69367-305
Miglitol	Miglitol 25 mg/1	Tablet, CoatedOral	Proficient Rx LP	71205-935
Miglitol	Miglitol 100 mg/1	Tablet, CoatedOral	Proficient Rx LP	71205-937