What is NDC 68071-3612?

68071-3612 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.

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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Bimatoprost NDC 68071-3612 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-3612Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-3612Add 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	Copy
68071-3612-5	6807136120568071361205	1 BOTTLE in 1 CARTON (68071-3612-5) / 2.5 mL in 1 BOTTLEMarketed from May 30, 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 202505
Marketing start: Mar 15, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Prostaglandins (Chemical structure)
Identifiers: Product ID 68071-3612_47fb98f0-c375-ec26-e063-6294a90aeeabSPL ID 47fb98f0-c375-ec26-e063-6294a90aeeabSPL set ID 19b21ff7-847c-3dc9-e063-6394a90a20ccRxCUI 308739UNII QXS94885MZUPC 0368071361254
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

N468071361205 followed by a unit qualifier and the quantity

Package 68071-3612-05. 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 Jan 9, 2026.

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 68071-3612

What is NDC 68071-3612?: 68071-3612 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Bimatoprost	Bimatoprost .1 mg/mL	Solution/ dropsOphthalmic	First Nation Group, LLC	81469-291	81469-0291-0581469-0291-25
Bimatoprost	Bimatoprost .1 mg/mL	Solution/ dropsOphthalmic	Lifestar Pharma LLC	70756-626	70756-0626-30
Bimatoprost	Bimatoprost .1 mg/mL	Solution/ dropsOphthalmic	Lifestar Pharma LLC	70756-627	70756-0627-30
Bimatoprost	Bimatoprost .1 mg/mL	Solution/ dropsOphthalmic	Lifestar Pharma LLC	70756-628	70756-0628-30
Bimatoprost	Bimatoprost .3 mg/mL	Solution/ dropsOphthalmic	Fosun Pharma USA Inc.	72266-241	72266-0241-01
Bimatoprost	Bimatoprost .1 mg/mL	Solution/ dropsOphthalmic	Amneal Pharmaceuticals NY LLC	60219-2149	60219-2149-0160219-2149-0260219-2149-04
bimatoprost	Bimatoprost .3 mg/mL	Solution/ dropsOphthalmic	Alembic Pharmaceuticals Limited	46708-511	46708-0511-0346708-0511-05
Bimatoprost	Bimatoprost .3 mg/mL	Solution/ dropsOphthalmic	Aurobindo Pharma Limited	65862-802	65862-0802-0565862-0802-1065862-0802-44
Bimatoprost	Bimatoprost .3 mg/mL	Solution/ dropsOphthalmic	Micro Labs Limited	42571-128	42571-0128-2142571-0128-2842571-0128-35
Bimatoprost	Bimatoprost .3 mg/mL	Solution/ dropsOphthalmic	Gland Pharma Limited	68083-439	68083-0439-01

All 24 Bimatoprost NDCs

Other NDCs under ANDA 202505

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

FDA NDC Directory listings under ANDA 202505
Product	Strength	Form · route	Labeler	Product NDC
Bimatoprost	Bimatoprost .3 mg/mL	Solution/ dropsOphthalmic	Micro Labs Limited	42571-128