Fosinopril inactive ingredients by manufacturer
Wondering whether your Fosinopril 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 Fosinopril 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 16 of the 19 current Fosinopril products on the market today, from 7 companies listing it with the FDA, and lined them up side by side. 3 are still being read and will appear on a later visit.
Ask about your bottle
Is there something in your Fosinopril? 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 Fosinopril products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseEvery checked product
Every checked Fosinopril product (16) lists lactose. See the products
-
Wheat or gluten sourceNo checked product
No checked Fosinopril product lists a wheat or gluten source.
-
SoyNo checked product
No checked Fosinopril product lists soy.
-
Synthetic dyesNo checked product
No checked Fosinopril product lists synthetic dyes.
-
GelatinNo checked product
No checked Fosinopril product lists gelatin.
Find a version without it
Every current Fosinopril product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| A-S Medication Solutions 2 products | ||
| 10 mg tabletNDC 50090-2977-00 | Lactose |
Show 5 ingredientsCROSPOVIDONE, LACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POVIDONE, UNSPECIFIED |
| 40 mg tabletNDC 50090-4743-00 | Lactose |
Show 5 ingredientsCROSPOVIDONE (15 MPA.S AT 5%), LACTOSE MONOHYDRATE, MICROCRYSTALLINE CELLULOSE, POVIDONE K29/32, SODIUM STEARYL FUMARATE |
| Aurobindo Pharma Limited 3 products | ||
| 10 mg tabletNDC 65862-0471-30 | Lactose |
Show 5 ingredientsANHYDROUS LACTOSE, CROSPOVIDONE, MICROCRYSTALLINE CELLULOSE, POVIDONE K30, SODIUM STEARYL FUMARATE |
| 20 mg tabletNDC 65862-0472-30 | Lactose |
Show 5 ingredientsANHYDROUS LACTOSE, CROSPOVIDONE, MICROCRYSTALLINE CELLULOSE, POVIDONE K30, SODIUM STEARYL FUMARATE |
| 40 mg tabletNDC 65862-0473-22 | Lactose |
Show 5 ingredientsANHYDROUS LACTOSE, CROSPOVIDONE, MICROCRYSTALLINE CELLULOSE, POVIDONE K30, SODIUM STEARYL FUMARATE |
| Bryant Ranch Prepack 3 products | ||
| 10 mg tabletNDC 71335-0381-01 | Lactose |
Show 5 ingredientsCROSPOVIDONE, LACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POVIDONE, UNSPECIFIED |
| 20 mg tabletNDC 71335-0187-01 | Lactose |
Show 5 ingredientsCROSPOVIDONE, LACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POVIDONE, UNSPECIFIED |
| 40 mg tabletNDC 71335-9703-01 | Still being read | Not read yet |
| Chartwell RX, LLC 3 products | ||
| 10 mg tabletNDC 62135-0041-90 | Lactose |
Show 5 ingredientsANHYDROUS LACTOSE, CARNAUBA WAX, CROSPOVIDONE, MICROCRYSTALLINE CELLULOSE, ZINC STEARATE |
| 20 mg tabletNDC 62135-0042-90 | Lactose |
Show 5 ingredientsANHYDROUS LACTOSE, CARNAUBA WAX, CROSPOVIDONE, MICROCRYSTALLINE CELLULOSE, ZINC STEARATE |
| 40 mg tabletNDC 62135-0043-90 | Lactose |
Show 5 ingredientsANHYDROUS LACTOSE, CARNAUBA WAX, CROSPOVIDONE, MICROCRYSTALLINE CELLULOSE, ZINC STEARATE |
| Cipla USA Inc. 3 products | ||
| 10 mg tabletNDC 69097-0856-05 | Lactose |
Show 5 ingredientsCROSPOVIDONE, UNSPECIFIED, LACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POVIDONE, UNSPECIFIED |
| 20 mg tabletNDC 69097-0857-05 | Lactose |
Show 5 ingredientsCROSPOVIDONE, UNSPECIFIED, LACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POVIDONE, UNSPECIFIED |
| 40 mg tabletNDC 69097-0858-05 | Still being read | Not read yet |
| Exelan Pharmaceuticals, Inc. 3 products | ||
| 10 mg tabletNDC 76282-0200-10 | Lactose |
Show 5 ingredientsCROSPOVIDONE, UNSPECIFIED, LACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POVIDONE, UNSPECIFIED |
| 20 mg tabletNDC 76282-0201-10 | Lactose |
Show 5 ingredientsCROSPOVIDONE, UNSPECIFIED, LACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POVIDONE, UNSPECIFIED |
| 40 mg tabletNDC 76282-0202-10 | Lactose |
Show 5 ingredientsCROSPOVIDONE, UNSPECIFIED, LACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POVIDONE, UNSPECIFIED |
| Solco Healthcare LLC 2 products | ||
| 20 mg tabletNDC 43547-0387-09 | Still being read | Not read yet |
| 40 mg tabletNDC 43547-0388-09 | Lactose |
Show 5 ingredientsCROSPOVIDONE (120 .MU.M), LACTOSE MONOHYDRATE, MICROCRYSTALLINE CELLULOSE, POVIDONE K30, SODIUM STEARYL FUMARATE |
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.
Fosinopril and lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. Every checked Fosinopril product (16) lists lactose.
Lists lactose
- A-S Medication Solutions: 10 mg tablet, 40 mg tablet
- Aurobindo: 10 mg tablet, 20 mg tablet, 40 mg tablet
- Bryant Ranch Prepack: 10 mg tablet, 20 mg tablet
- Chartwell RX: 10 mg tablet, 20 mg tablet, 40 mg tablet
- Cipla: 10 mg tablet, 20 mg tablet
- Exelan: 10 mg tablet, 20 mg tablet, 40 mg tablet
- Solco Healthcare: 40 mg tablet
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.
Common questions about Fosinopril inactive ingredients
Is Fosinopril gluten-free?
Does Fosinopril contain lactose?
Does Fosinopril contain soy?
Is there a dye-free Fosinopril?
Does Fosinopril contain gelatin?
Why do the inactive ingredients differ between manufacturers?
Can my pharmacy give me a specific manufacturer's version?
How current is this list?
Sources: the products are the finished Fosinopril products in the FDA's current NDC directory (openFDA), as of October 5, 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 Fosinopril guide