NDC codes

FDA NDC Directory
Product NDC (as listed)71205-072Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0072Add 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
71205-072-30712050072307120500723030 TABLET in 1 BOTTLE (71205-072-30)Marketed from Jul 2, 2018
71205-072-60712050072607120500726060 TABLET in 1 BOTTLE (71205-072-60)Marketed from Jul 2, 2018
71205-072-90712050072907120500729090 TABLET in 1 BOTTLE (71205-072-90)Marketed from Jul 2, 2018

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)
HydrALAZINE Hydrochloride
Generic name (nonproprietary)
hydralazine hydrochloride
Active ingredients
Hydralazine hydrochloride — 50 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 71205
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 200770
Marketing start
Listing expires
Other FDA classes
Arteriolar Vasodilation (Physiologic effect)
Identifiers
Product ID 71205-072_5696b87a-c388-4cd2-b22b-b2861c28d800SPL ID 5696b87a-c388-4cd2-b22b-b2861c28d800SPL set ID dfd60a79-2a30-41e6-b000-a144730099a8RxCUI 905395UNII FD171B778Y
Pharmacologic class
Arteriolar Vasodilator

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

N471205007230 followed by a unit qualifier and the quantity

Package 71205-0072-30. 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 Essential hypertension, alone or as an adjunct.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-072

What is NDC 71205-072?
71205-072 is the product NDC for HydrALAZINE Hydrochloride, Hydralazine hydrochloride 50 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
HydrALAZINE Hydrochloride.
What is the active ingredient?
Hydralazine hydrochloride.
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 HydrALAZINE Hydrochloride?
144 other product NDCs are listed under this name. See all HydrALAZINE Hydrochloride 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 HydrALAZINE Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Hydralazine HydrochlorideHydralazine hydrochloride 50 mg/1TabletOralCardinal Health 107, LLC55154-028755154-0287-00
HydrALAZINE HydrochlorideHydralazine hydrochloride 50 mg/1TabletOralCoupler LLC67046-208067046-2080-03
Hydralazine HydrochlorideHydralazine hydrochloride 10 mg/1TabletOralSafecor Health, LLC48433-04648433-0046-20
Hydralazine HydrochlorideHydralazine hydrochloride 25 mg/1TabletOralSafecor Health, LLC48433-04748433-0047-20
Hydralazine HydrochlorideHydralazine hydrochloride 50 mg/1TabletOralSafecor Health, LLC48433-04848433-0048-20
Hydralazine HydrochlorideHydralazine hydrochloride 25 mg/1TabletOralCoupler LLC67046-166067046-1660-03
Hydralazine HydrochlorideHydralazine hydrochloride 20 mg/mLInjectionIntramuscular, IntravenousNavinta LLC68475-51468475-0514-02
Hydralazine HydrochlorideHydralazine hydrochloride 10 mg/1TabletOralCoupler LLC67046-160967046-1609-03
Hydralazine HydrochlorideHydralazine hydrochloride 20 mg/mLInjectionIntramuscular, IntravenousBaxter Healthcare Corporation43066-04143066-0041-25
Hydralazine HydrochlorideHydralazine hydrochloride 25 mg/1TabletOralCardinal Health 107, LLC55154-018655154-0186-00

All 145 HydrALAZINE Hydrochloride NDCs

Other NDCs under ANDA 200770

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

FDA NDC Directory listings under ANDA 200770
ProductStrengthForm · routeLabelerProduct NDC
HydrALAZINE HydrochlorideHydralazine hydrochloride 10 mg/1TabletOralStrides Pharma Science Limited64380-733
HydrALAZINE HydrochlorideHydralazine hydrochloride 25 mg/1TabletOralStrides Pharma Science Limited64380-734
HydrALAZINE HydrochlorideHydralazine hydrochloride 50 mg/1TabletOralStrides Pharma Science Limited64380-735
HydrALAZINE HydrochlorideHydralazine hydrochloride 100 mg/1TabletOralStrides Pharma Science Limited64380-736
HydrALAZINE HydrochlorideHydralazine hydrochloride 50 mg/1TabletOralCoupler LLC67046-2080

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