NDC codes

FDA NDC Directory
Product NDC (as listed)71872-7080Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71872-7080Add 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
71872-7080-171872708001718727080011 VIAL in 1 BAG (71872-7080-1) / 1 mL in 1 VIALMarketed from Mar 6, 2018

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

Brand name (proprietary)
Terbutaline Sulfate
Generic name (nonproprietary)
terbutaline sulfate
Active ingredients
Terbutaline sulfate — 1 mg/mL
Dosage form
Injection
Route
Subcutaneous
Labeler
Medical Purchasing Solutions. LLCNDC labeler code 71872
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078630
Marketing start
Listing expires
Identifiers
Product ID 71872-7080_fc5fc617-c901-4ee6-e053-6294a90aeb43SPL ID fc5fc617-c901-4ee6-e053-6294a90aeb43SPL set ID 6a22b62c-4ee1-49df-e053-2a91aa0a3e52RxCUI 857635UNII 576PU70Y8E

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

N471872708001 followed by a unit qualifier and the quantity

Package 71872-7080-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Terbutaline Sulfate Injection, USP is indicated for the prevention and reversal of bronchospasm in patients 12 years of age and older with asthma and reversible bronchospasm associated with bronchitis and emphysema.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71872-7080

What is NDC 71872-7080?
71872-7080 is the product NDC for Terbutaline Sulfate, Terbutaline sulfate 1 mg/mL injection, listed with the FDA by Medical Purchasing Solutions. LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Terbutaline Sulfate.
What is the active ingredient?
Terbutaline sulfate.
Who is the labeler?
Medical Purchasing Solutions. LLC, NDC labeler code 71872. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Terbutaline Sulfate?
16 other product NDCs are listed under this name. See all Terbutaline 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 Terbutaline Sulfate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Terbutaline SulfateTerbutaline sulfate 1 mg/mLInjection, SolutionSubcutaneousHenry Schein, Inc.0404-996200404-9962-01
Terbutaline SulfateTerbutaline sulfate 2.5 mg/1TabletOralUpsher-Smith Laboratories, LLC24979-13224979-0132-0124979-0132-03
Terbutaline SulfateTerbutaline sulfate 5 mg/1TabletOralUpsher-Smith Laboratories, LLC24979-13324979-0133-0124979-0133-03
Terbutaline SulfateTerbutaline sulfate 2.5 mg/1TabletOralProficient Rx LP71205-93871205-0938-0071205-0938-3071205-0938-55+2 more
Terbutaline SulfateTerbutaline sulfate 5 mg/1TabletOralProficient Rx LP71205-93971205-0939-0071205-0939-3071205-0939-55+2 more
Terbutaline SulfateTerbutaline sulfate 2.5 mg/1TabletOralANI Pharmaceuticals, Inc.62559-72162559-0721-01
Terbutaline SulfateTerbutaline sulfate 5 mg/1TabletOralANI Pharmaceuticals, Inc.62559-72262559-0722-01
Terbutaline SulfateTerbutaline sulfate 1 mg/mLInjection, SolutionSubcutaneousFresenius Kabi USA, LLC63323-66563323-0665-01
Terbutaline SulfateTerbutaline sulfate 1 mg/mLInjectionSubcutaneousHikma Pharmaceuticals USA Inc.0143-937500143-9375-10
Terbutaline SulfateTerbutaline sulfate 1 mg/mLInjectionSubcutaneousHikma Pharmaceuticals USA Inc.0143-974600143-9746-10

All 17 Terbutaline Sulfate NDCs

Other NDCs under ANDA 078630

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

FDA NDC Directory listings under ANDA 078630
ProductStrengthForm · routeLabelerProduct NDC
Terbutaline SulfateTerbutaline sulfate 1 mg/mLInjectionSubcutaneousHikma Pharmaceuticals USA Inc.0143-9375
Terbutaline SulfateTerbutaline sulfate 1 mg/mLInjectionSubcutaneousHikma Pharmaceuticals USA Inc.0143-9746

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