Atropine inactive ingredients by manufacturer

Name: Atropine Inactive Ingredients by Manufacturer
Creator: HelloPharmacist

Wondering whether your Atropine has lactose, gluten, soy, a dye or gelatin in it? The medicine is the same, but the fillers, coatings and colors differ from one company to the next. This page shows what each Atropine product's FDA label lists, so you can find a version that leaves out what you avoid and ask your pharmacist for it by its NDC.

We have read the FDA labels of 77 of the 78 current Atropine products on the market today, from 30 companies listing it with the FDA, and lined them up side by side. 1 label has no inactive-ingredient list we could read, so that product cannot be compared.

Ask about your bottle

Is there something in your Atropine? Ask in plain words.

Name the company, strength or the NDC on your bottle and the ingredient you avoid. The answer comes only from the FDA labels on this page.

Answers are drawn from the FDA label data on this page and checked against it. They are not medical advice: confirm with your pharmacist before relying on them.

The short answer

Which Atropine products list lactose, a gluten source, soy, dyes or gelatin?

LactoseNo checked product

No checked Atropine product lists lactose.
Wheat or gluten sourceNo checked product

No checked Atropine product lists a wheat or gluten source.
SoyNo checked product

No checked Atropine product lists soy.
Synthetic dyesNo checked product

No checked Atropine product lists synthetic dyes.
GelatinNo checked product

No checked Atropine product lists gelatin.

Also listed by some products: Benzyl alcohol 13 of 77

Find a version without it

Every current Atropine product and what its label lists

Hide products that list:

Product	Lists	Inactive ingredients on the label
A-S Medication Solutions 3 products
10 mg/mL eye dropsNDC 50090-7000-00	None of these listed	Show 8 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER
10 mg/mL eye dropsNDC 50090-7313-00	None of these listed	Show 8 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
0.1 mg/mL injectionNDC 50090-5924-00	None of these listed	Show 3 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID
Accord Healthcare, Inc., 2 products
0.05 mg/mL injectionNDC 16729-0483-03	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.1 mg/mL injectionNDC 16729-0484-03	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Accord Healthcare Inc. 1 product
0.4 mg/mL injectionNDC 16729-0512-43	Benzyl alcohol	Show 4 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
Alcon Laboratories, Inc. 2 products
10 mg/mL eye dropsNDC 00065-0303-55	None of these listed	Show 6 ingredients Benzalkonium Chloride, Boric Acid, Hydrochloric Acid, Hypromelloses, Sodium Hydroxide, Water
10 mg/mL eye dropsNDC 00065-0817-01	None of these listed	Show 6 ingredients Benzalkonium Chloride, Boric Acid, Hydrochloric Acid, Hypromellose, Unspecified, Sodium Hydroxide, Water
American Regent, Inc. 2 products
0.4 mg/mL injectionNDC 00517-1004-25	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
1 mg/mL injectionNDC 00517-1001-25	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Amneal Pharmaceuticals LLC 2 products
0.1 mg/mL injectionNDC 70121-1705-07	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.1 mg/mL injectionNDC 70121-1706-01	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Amneal Pharmaceuticals NY LLC 3 products
10 mg/mL eye dropsNDC 60219-1748-02	None of these listed	Show 8 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
10 mg/mL eye dropsNDC 60219-1749-03	None of these listed	Show 8 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
10 mg/mL eye dropsNDC 60219-1750-08	None of these listed	Show 8 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
Apotex Corp. 1 product
10 mg/mL eye dropsNDC 60505-6226-00	None of these listed	Show 8 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER
Bausch & Lomb Incorporated 2 products
10 mg/mL eye dropsNDC 24208-0965-01	None of these listed	Show 5 ingredients BORIC ACID, HYDROCHLORIC ACID, HYPROMELLOSE, UNSPECIFIED, SODIUM HYDROXIDE, WATER
10 mg/g eye ointmentNDC 24208-0825-55	None of these listed	Show 4 ingredients LANOLIN OIL, MINERAL OIL, PETROLATUM, WATER
Bausch & Lomb Americas Inc. 1 product
10 mg/mL eye dropsNDC 82260-0001-01	None of these listed	Show 5 ingredients BORIC ACID, HYDROCHLORIC ACID, HYPROMELLOSE, UNSPECIFIED, SODIUM HYDROXIDE, WATER
Edenbridge Pharmaceuticals LLC. 1 product
10 mg/mL eye dropsNDC 42799-0826-01	None of these listed	Show 8 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
Fresenius Kabi USA, LLC 1 product
0.4 mg/mL injectionNDC 63323-0580-20	Benzyl alcohol	Show 4 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
Gland Pharma Limited 3 products
10 mg/mL eye dropsNDC 68083-0669-01	None of these listed	Show 8 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
10 mg/mL eye dropsNDC 68083-0670-01	None of these listed	Show 8 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
10 mg/mL eye dropsNDC 68083-0671-01	None of these listed	Show 8 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
Henry Schein, Inc 1 product
0.4 mg/mL injectionNDC 00404-9802-01	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, Water
Henry Schein, Inc. 3 products
0.05 mg/mL injectionNDC 00404-9823-05	No inactive-ingredient list on the label	No list we could read
0.1 mg/mL injectionNDC 00404-9784-05	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 00404-9804-20	Benzyl alcohol	Show 4 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
HF Acquisition Co., LLC, DBA Health First 1 product
0.1 mg/mL injectionNDC 51662-1208-01	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
HF Acquisition Co. LLC, DBA Health First 1 product
0.1 mg/mL injectionNDC 51662-1207-01	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
HF Acquisition Co LLC, DBA HealthFirst 6 products
0.1 mg/mL injectionNDC 51662-1527-01	None of these listed	Show 3 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID
0.1 mg/mL injectionNDC 51662-1289-01	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 51662-1311-01	Benzyl alcohol	Show 4 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 51662-1619-01	Benzyl alcohol	Show 3 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID
0.4 mg/mL injectionNDC 51662-1627-03	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
1 mg/mL injectionNDC 51662-1626-03	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Hikma Pharmaceuticals USA Inc. 3 products
0.4 mg/mL injectionNDC 00641-6251-10	Benzyl alcohol	Show 3 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID
0.4 mg/mL injectionNDC 00641-6274-25	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
1 mg/mL injectionNDC 00641-6275-25	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Hospira, Inc. 2 products
0.05 mg/mL injectionNDC 00409-9630-05	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.1 mg/mL injectionNDC 00409-1630-10	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
International Medication Systems, Limited 1 product
0.1 mg/mL injectionNDC 76329-3340-01	None of these listed	Show 3 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID
Lifestar Pharma LLC 3 products
10 mg/mL eye dropsNDC 70756-0651-25	None of these listed	Show 7 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 70756-0652-25	None of these listed	Show 7 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 70756-0653-35	None of these listed	Show 7 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
Medefil, Inc. 1 product
0.1 mg/mL injectionNDC 64253-0400-91	None of these listed	Show 1 ingredient SODIUM CHLORIDE
Medical Purchasing Solutions, LLC 9 products
0.1 mg/mL injectionNDC 71872-7252-01	None of these listed	Show 3 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID
0.1 mg/mL injectionNDC 71872-7298-01	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.1 mg/mL injectionNDC 71872-7002-01	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 71872-7037-01	Benzyl alcohol	Show 4 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 71872-7316-01	Benzyl alcohol	Show 3 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID
0.4 mg/mL injectionNDC 71872-7312-01	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 71872-7341-01	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 71872-7355-01	Benzyl alcohol	Show 4 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
1 mg/mL injectionNDC 71872-7340-01	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Meridian Medical Technologies LLC 5 products
0.5 mg/0.7 mL injectionNDC 11704-0104-01	None of these listed	Show 6 ingredients citric acid monohydrate, glycerin, Nitrogen, phenol, sodium citrate, unspecified form, water
0.25 mg/0.3 mL injectionNDC 11704-0107-01	None of these listed	Show 5 ingredients citric acid monohydrate, Nitrogen, sodium chloride, sodium citrate, unspecified form, water
1 mg/0.7 mL injectionNDC 11704-0105-01	None of these listed	Show 6 ingredients citric acid monohydrate, glycerin, Nitrogen, phenol, sodium citrate, unspecified form, water
2 mg/0.7 mL injectionNDC 11704-0101-01	None of these listed	Show 6 ingredients citric acid monohydrate, glycerin, Nitrogen, phenol, sodium citrate, unspecified form, water
2 mg/0.7 mL injectionNDC 11704-0106-01	None of these listed	Show 6 ingredients citric acid monohydrate, glycerin, Nitrogen, phenol, sodium citrate, unspecified form, water
NorthStar RxLLC 1 product
10 mg/mL eye dropsNDC 72603-0264-01	None of these listed	Show 7 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
ProPharma Distribution 5 products
0.1 mg/mL injectionNDC 84549-0340-01	None of these listed	Show 3 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID
0.1 mg/mL injectionNDC 84549-0400-91	None of these listed	Show 1 ingredient SODIUM CHLORIDE
0.4 mg/mL injectionNDC 84549-0580-20	Benzyl alcohol	Show 4 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 84549-0631-25	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
1 mg/mL injectionNDC 84549-0001-25	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Redpharm Drug 2 products
10 mg/mL eye dropsNDC 67296-2124-05	None of these listed	Show 7 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 67296-2200-05	None of these listed	Show 8 ingredients BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER
Remedyrepack Inc. 3 products
0.1 mg/mL injectionNDC 70518-3120-00	None of these listed	Show 3 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID
0.4 mg/mL injectionNDC 70518-4329-00	Benzyl alcohol	Show 3 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID
0.4 mg/mL injectionNDC 70518-4188-00	Benzyl alcohol	Show 4 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
Somerset Therapeutics, LLC 7 products
10 mg/mL eye dropsNDC 70069-0581-01	None of these listed	Show 6 ingredients BENZALKONIUM CHLORIDE, EDETATE SODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 70069-0582-01	None of these listed	Show 6 ingredients BENZALKONIUM CHLORIDE, EDETATE SODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 70069-0583-01	None of these listed	Show 6 ingredients BENZALKONIUM CHLORIDE, EDETATE SODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 70069-0716-01	None of these listed	Show 6 ingredients BENZALKONIUM CHLORIDE, BORIC ACID, HYDROCHLORIC ACID, HYPROMELLOSE, UNSPECIFIED, SODIUM HYDROXIDE, WATER
0.4 mg/mL injectionNDC 70069-0481-10	Benzyl alcohol	Show 4 ingredients BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 70069-0631-25	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
1 mg/mL injectionNDC 70069-0641-25	None of these listed	Show 4 ingredients SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER

A product with none of these listed is not certified to be without them: the label says what the manufacturer declared, and the source of a starch or a flavor is often not stated. The companies are the FDA's labelers, which include repackagers and distributors selling another company's product under their own label. The NDC opens the product's own page, with the full label and its inactive-ingredient notes.

Atropine without benzyl alcohol

Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 13 of 77 checked products list benzyl alcohol; 64 do not.

Does not list benzyl alcohol

A-S Medication Solutions: 10 mg/mL eye drops (NDC 50090-7000-00), 10 mg/mL eye drops (NDC 50090-7313-00), 0.1 mg/mL injection
Accord Healthcare, Inc.,: 0.05 mg/mL injection, 0.1 mg/mL injection
Alcon: 10 mg/mL eye drops (NDC 00065-0303-55), 10 mg/mL eye drops (NDC 00065-0817-01)
American Regent: 0.4 mg/mL injection, 1 mg/mL injection
Amneal Pharmaceuticals LLC: 0.1 mg/mL injection (NDC 70121-1705-07), 0.1 mg/mL injection (NDC 70121-1706-01)
Amneal Pharmaceuticals NY LLC: 10 mg/mL eye drops (NDC 60219-1748-02), 10 mg/mL eye drops (NDC 60219-1749-03), 10 mg/mL eye drops (NDC 60219-1750-08)
Apotex: 10 mg/mL eye drops
Bausch & Lomb: 10 mg/mL eye drops, 10 mg/g eye ointment
Bausch & Lomb Americas: 10 mg/mL eye drops
Edenbridge: 10 mg/mL eye drops
Gland: 10 mg/mL eye drops (NDC 68083-0669-01), 10 mg/mL eye drops (NDC 68083-0670-01), 10 mg/mL eye drops (NDC 68083-0671-01)
Henry Schein, Inc: 0.4 mg/mL injection
Henry Schein, Inc.: 0.1 mg/mL injection
HF Acquisition Co., LLC, DBA Health First: 0.1 mg/mL injection
HF Acquisition Co. LLC, DBA Health First: 0.1 mg/mL injection
HF Acquisition Co LLC, DBA HealthFirst: 0.1 mg/mL injection (NDC 51662-1527-01), 0.1 mg/mL injection (NDC 51662-1289-01), 0.4 mg/mL injection, 1 mg/mL injection
Hikma: 0.4 mg/mL injection, 1 mg/mL injection
Hospira: 0.05 mg/mL injection, 0.1 mg/mL injection
International Medication Systems: 0.1 mg/mL injection
Lifestar: 10 mg/mL eye drops (NDC 70756-0651-25), 10 mg/mL eye drops (NDC 70756-0652-25), 10 mg/mL eye drops (NDC 70756-0653-35)
Medefil: 0.1 mg/mL injection
Medical Purchasing Solutions: 0.1 mg/mL injection (NDC 71872-7252-01), 0.1 mg/mL injection (NDC 71872-7298-01), 0.1 mg/mL injection (NDC 71872-7002-01), 0.4 mg/mL injection (NDC 71872-7312-01), 0.4 mg/mL injection (NDC 71872-7341-01), 1 mg/mL injection
Meridian Medical Technologies: 0.5 mg/0.7 mL injection, 0.25 mg/0.3 mL injection, 1 mg/0.7 mL injection, 2 mg/0.7 mL injection (NDC 11704-0101-01), 2 mg/0.7 mL injection (NDC 11704-0106-01)
NorthStar RxLLC: 10 mg/mL eye drops
ProPharma Distribution: 0.1 mg/mL injection (NDC 84549-0340-01), 0.1 mg/mL injection (NDC 84549-0400-91), 0.4 mg/mL injection, 1 mg/mL injection
Redpharm Drug: 10 mg/mL eye drops (NDC 67296-2124-05), 10 mg/mL eye drops (NDC 67296-2200-05)
Remedyrepack: 0.1 mg/mL injection
Somerset Therapeutics: 10 mg/mL eye drops (NDC 70069-0581-01), 10 mg/mL eye drops (NDC 70069-0582-01), 10 mg/mL eye drops (NDC 70069-0583-01), 10 mg/mL eye drops (NDC 70069-0716-01), 0.4 mg/mL injection, 1 mg/mL injection

Lists benzyl alcohol

Accord Healthcare Inc.: 0.4 mg/mL injection
Fresenius Kabi: 0.4 mg/mL injection
Henry Schein, Inc.: 0.4 mg/mL injection
HF Acquisition Co LLC, DBA HealthFirst: 0.4 mg/mL injection (NDC 51662-1311-01), 0.4 mg/mL injection (NDC 51662-1619-01)
Hikma: 0.4 mg/mL injection
Medical Purchasing Solutions: 0.4 mg/mL injection (NDC 71872-7037-01), 0.4 mg/mL injection (NDC 71872-7316-01), 0.4 mg/mL injection (NDC 71872-7355-01)
ProPharma Distribution: 0.4 mg/mL injection
Remedyrepack: 0.4 mg/mL injection (NDC 70518-4329-00), 0.4 mg/mL injection (NDC 70518-4188-00)
Somerset Therapeutics: 0.4 mg/mL injection

At the pharmacy counter

How to use this at the pharmacy counter

Pick the company whose list suits you and copy the NDC from the table. Many pharmacies order from wholesalers that carry several companies' versions and can request a particular one if you ask before the prescription is filled; some buy from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check.
Treat "does not list" as exactly that. The label is what the manufacturer declared; a flavor or a starch may have an unstated source, and lines change. For celiac disease or a serious allergy, ask the manufacturer's medical information line for a written statement about the lot you have.
Check the bottle each refill. A different company usually means a different shape, color and inactive-ingredient list; the pharmacist can tell you who made it, and the two-NDC comparison shows the difference line by line.
If you need one company's version kept constant, ask your prescriber to write that company or the NDC on the prescription and tell the pharmacy you need it held. Rules vary by state and plan, so confirm with the pharmacist.

Ask Dr. Staiger which Atropine product suits you →

Common questions about Atropine inactive ingredients

Is Atropine gluten-free?

This page cannot certify any Atropine product gluten-free; it reports what each label declares. Of the 77 products checked, none lists a wheat, barley, rye or gluten ingredient, and none lists a starch without a stated source. If you have celiac disease, ask the manufacturer's medical information line for a written gluten statement for the lot you have.

Does Atropine contain lactose?

No checked Atropine product lists lactose on its label. People with a milk allergy or a strong intolerance often prefer a version that does not list it.

Does Atropine contain soy?

No checked Atropine product lists a soy ingredient (soybean oil or soy lecithin) on its label. Soy lecithin is the usual form and the amount is small, but people with a soy allergy often prefer a version that does not list it.

Is there a dye-free Atropine?

No checked Atropine product lists a synthetic dye (an FD&C or D&C colorant) on its label. Colorants often differ by strength within one company's line, so compare the lists above strength by strength.

Does Atropine contain gelatin?

No checked Atropine product lists gelatin on its label. Gelatin is usually bovine or porcine and the label rarely says which; for kosher, halal or vegetarian needs, ask the manufacturer.

Why do the inactive ingredients differ between manufacturers?

A generic must match the brand's active ingredient, strength, dose form and how it is absorbed; its fillers, binders, coatings and colorants are the manufacturer's own choice. That is why one Atropine product can list lactose and a dye while another from a different company lists neither.

Can my pharmacy give me a specific manufacturer's version?

Often, if you ask before the prescription is filled: many pharmacies order from wholesalers that carry several companies' versions and can request a particular one. Some pharmacies buy a generic from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check. Give them the NDC from this page; the company name alone is often enough.

How current is this list?

The products are the ones in the FDA's current NDC directory as of October 6, 2026, and each inactive-ingredient list is the manufacturer's FDA label as our label sync last read it. Formulations change, so check the label on your own bottle and ask your pharmacist if a refill looks different.

Sources: the products are the finished Atropine products in the FDA's current NDC directory (openFDA), as of October 6, 2026; each inactive-ingredient list is the manufacturer's FDA Structured Product Label via DailyMed, as our label sync last read it. The concern groups are HelloPharmacist's classification of the names the label declares. Educational information only, not medical advice; confirm with your pharmacist before relying on a list. ← Back to the Atropine guide