NDC codes

FDA NDC Directory
Product NDC (as listed)68071-3590Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-3590Add 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
68071-3590-568071359005680713590051 BOTTLE in 1 CARTON (68071-3590-5) / 2.5 mL in 1 BOTTLEMarketed from Mar 25, 2024

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)
Bimatoprost
Generic name (nonproprietary)
bimatoprost
Active ingredients
Bimatoprost — .3 mg/mL
Dosage form
Solution/ drops
Route
Ophthalmic
Labeler
NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210126
Marketing start
Listing expires
Other FDA classes
Prostaglandins (Chemical structure)
Identifiers
Product ID 68071-3590_147e1501-382d-e443-e063-6294a90ac5a8SPL ID 147e1501-382d-e443-e063-6294a90ac5a8SPL set ID 147e2ec6-8fb1-ed5a-e063-6294a90a5ecaRxCUI 308739UNII QXS94885MZUPC 0368071359053
Pharmacologic class
Prostaglandin Analog

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. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468071359005 followed by a unit qualifier and the quantity

Package 68071-3590-05. 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)

Bimatoprost ophthalmic solution, 0.03% is indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension. Bimatoprost ophthalmic solution, 0.03% is a prostaglandin analog indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension. (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68071-3590

What is NDC 68071-3590?
68071-3590 is the product NDC for Bimatoprost, Bimatoprost .3 mg/mL solution/ drops, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Bimatoprost.
What is the active ingredient?
Bimatoprost.
Who is the labeler?
NuCare Pharmaceuticals,Inc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bimatoprost?
23 other product NDCs are listed under this name. See all Bimatoprost 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 Bimatoprost NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
BimatoprostBimatoprost .1 mg/mLSolution/ dropsOphthalmicFirst Nation Group, LLC81469-29181469-0291-0581469-0291-25
BimatoprostBimatoprost .1 mg/mLSolution/ dropsOphthalmicLifestar Pharma LLC70756-62670756-0626-30
BimatoprostBimatoprost .1 mg/mLSolution/ dropsOphthalmicLifestar Pharma LLC70756-62770756-0627-30
BimatoprostBimatoprost .1 mg/mLSolution/ dropsOphthalmicLifestar Pharma LLC70756-62870756-0628-30
BimatoprostBimatoprost .3 mg/mLSolution/ dropsOphthalmicFosun Pharma USA Inc.72266-24172266-0241-01
BimatoprostBimatoprost .1 mg/mLSolution/ dropsOphthalmicAmneal Pharmaceuticals NY LLC60219-214960219-2149-0160219-2149-0260219-2149-04
bimatoprostBimatoprost .3 mg/mLSolution/ dropsOphthalmicAlembic Pharmaceuticals Limited46708-51146708-0511-0346708-0511-05
BimatoprostBimatoprost .3 mg/mLSolution/ dropsOphthalmicAurobindo Pharma Limited65862-80265862-0802-0565862-0802-1065862-0802-44
BimatoprostBimatoprost .3 mg/mLSolution/ dropsOphthalmicMicro Labs Limited42571-12842571-0128-2142571-0128-2842571-0128-35
BimatoprostBimatoprost .3 mg/mLSolution/ dropsOphthalmicNuCare Pharmaceuticals,Inc.68071-361268071-3612-05

All 24 Bimatoprost NDCs

Other NDCs under ANDA 210126

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

FDA NDC Directory listings under ANDA 210126
ProductStrengthForm · routeLabelerProduct NDC
BimatoprostBimatoprost .3 mg/mLSolution/ dropsOphthalmicGland Pharma Limited68083-296
BimatoprostBimatoprost .3 mg/mLSolution/ dropsOphthalmicGland Pharma Limited68083-295
BimatoprostBimatoprost .3 mg/mLSolution/ dropsOphthalmicFosun Pharma USA Inc.72266-140
BimatoprostBimatoprost .3 mg/mLSolution/ dropsOphthalmicFosun Pharma USA Inc.72266-139
BimatoprostBimatoprost .3 mg/mLSolution/ dropsOphthalmicFosun Pharma USA Inc.72266-241
BimatoprostBimatoprost .3 mg/mLSolution/ dropsOphthalmicGland Pharma Limited68083-439

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