Inactive ingredients by manufacturer

Meropenem inactive ingredients by manufacturer

Wondering whether your Meropenem 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 Meropenem 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 27 of the 43 current Meropenem products on the market today, from 18 companies listing it with the FDA, and lined them up side by side. 9 are still being read and will appear on a later visit. 7 labels have no inactive-ingredient list we could read, so those products cannot be compared.

Ask about your bottle

Is there something in your Meropenem? 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 Meropenem products list lactose, a gluten source, soy, dyes or gelatin?

  1. LactoseNo checked product

    No checked Meropenem product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Meropenem product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Meropenem product lists soy.

  4. Synthetic dyesNo checked product

    No checked Meropenem product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Meropenem product lists gelatin.

Find a version without it

Every current Meropenem product and what its label lists

No checked product lists any of the concerns we look for.

ProductListsInactive ingredients on the label
Amneal Pharmaceuticals LLC 2 products
1 g/30 mL injectionNDC 70121-1453-07 Still being read Not read yet
500 mg/20 mL injectionNDC 70121-1454-07 Still being read Not read yet
Armas Pharmaceuticals Inc 2 products
1 g/20 mL injectionNDC 72485-0412-01 None of these listed
Show 1 ingredient

SODIUM CARBONATE
500 mg/20 mL injectionNDC 72485-0411-01 None of these listed
Show 1 ingredient

SODIUM CARBONATE
BluePoint Laboratories 2 products
1 g/30 mL injectionNDC 68001-0324-57 None of these listed
Show 1 ingredient

SODIUM CARBONATE
500 mg/20 mL injectionNDC 68001-0323-31 Still being read Not read yet
Brooks Steriscience Limited 3 products
1 g/20 mL injectionNDC 81962-0001-01 None of these listed
Show 1 ingredient

SODIUM CARBONATE
2 g injectionNDC 81962-0002-08 None of these listed
Show 1 ingredient

SODIUM CARBONATE
500 mg/20 mL injectionNDC 81962-0000-01 None of these listed
Show 1 ingredient

SODIUM CARBONATE
Civica, Inc 2 products
1 g/30 mL injectionNDC 72572-0416-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
500 mg/20 mL injectionNDC 72572-0415-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
Civica, Inc. 2 products
1 g/20 mL injectionNDC 72572-0410-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
500 mg/20 mL injectionNDC 72572-0412-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
Eugia US LLC 2 products
1 g injectionNDC 55150-0208-30 None of these listed
Show 1 ingredient

SODIUM CARBONATE
500 mg injectionNDC 55150-0207-20 None of these listed
Show 1 ingredient

SODIUM CARBONATE
Fresenius Kabi USA, LLC 2 products
1 g/20 mL injectionNDC 63323-0508-25 No inactive-ingredient list on the label No list we could read
500 mg/10 mL injectionNDC 63323-0507-20 No inactive-ingredient list on the label No list we could read
Gland Pharma Limited 2 products
1 g/30 mL injectionNDC 68083-0147-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
500 mg/20 mL injectionNDC 68083-0146-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
Hikma Pharmaceuticals USA Inc. 4 products
1 g/20 mL injectionNDC 00143-9486-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
1 g/30 mL injectionNDC 00143-9431-10 Still being read Not read yet
500 mg/10 mL injectionNDC 00143-9485-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
500 mg/20 mL injectionNDC 00143-9430-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
Hospira, Inc. 4 products
1 g/20 mL injectionNDC 00409-1391-22 No inactive-ingredient list on the label No list we could read
1 g/20 mL injectionNDC 00409-3412-10 No inactive-ingredient list on the label No list we could read
500 mg/10 mL injectionNDC 00409-0222-10 No inactive-ingredient list on the label No list we could read
500 mg/10 mL injectionNDC 00409-1390-51 No inactive-ingredient list on the label No list we could read
Mylan Institutional LLC 1 product
2 g injectionNDC 72078-0081-06 None of these listed
Show 1 ingredient

SODIUM CARBONATE
Qilu Antibiotics Pharmaceutical Co., Ltd. 2 products
1 g/30 mL injectionNDC 51810-0503-02 Still being read Not read yet
500 mg/20 mL injectionNDC 51810-0502-02 None of these listed
Show 1 ingredient

SODIUM CARBONATE
Sagent Pharmaceuticals 2 products
1 g/30 mL injectionNDC 25021-0161-30 Still being read Not read yet
500 mg/20 mL injectionNDC 25021-0160-20 None of these listed
Show 1 ingredient

Sodium Carbonate
Sandoz Inc 2 products
1 g/30 mL injectionNDC 00781-3098-95 None of these listed
Show 1 ingredient

SODIUM CARBONATE
500 mg/20 mL injectionNDC 00781-3000-95 None of these listed
Show 1 ingredient

SODIUM CARBONATE
Savior Lifetec Corporation 2 products
1 g/30 mL injectionNDC 44647-0033-10 Still being read Not read yet
500 mg/20 mL injectionNDC 44647-0032-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
WG Critical Care, LLC 5 products
1 g injectionNDC 44567-0146-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
1 g injectionNDC 44567-0401-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
2 g injectionNDC 44567-0402-06 Still being read Not read yet
500 mg injectionNDC 44567-0145-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
500 mg injectionNDC 44567-0400-10 None of these listed
Show 1 ingredient

SODIUM CARBONATE
Xellia Pharmaceuticals USA LLC 2 products
1 g injectionNDC 70594-0076-02 Still being read Not read yet
500 mg injectionNDC 70594-0075-02 No inactive-ingredient list on the label No list we could read

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.

At the pharmacy counter

How to use this at the pharmacy counter

  1. 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.
  2. 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.
  3. 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.
  4. 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 Meropenem product suits you →

Common questions about Meropenem inactive ingredients

Is Meropenem gluten-free?
This page cannot certify any Meropenem product gluten-free; it reports what each label declares. Of the 27 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 Meropenem contain lactose?
No checked Meropenem 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 Meropenem contain soy?
No checked Meropenem 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 Meropenem?
No checked Meropenem 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 Meropenem contain gelatin?
No checked Meropenem 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 and dose form. For injectable, ophthalmic and otic products the FDA generally requires the inactive ingredients to match the reference product as well, so the lists on this page differ less than they do for tablets and capsules; the differences that remain come from the exact product and container each company files.
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 5, 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 Meropenem 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 Meropenem guide