FDA Label Search
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NDC Search Results on Proprietary Name: gemcitabine
Click on Proprietary Name to view the label.
| Proprietary Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
|---|---|---|---|---|---|
| Gemcitabine hydrochloride | 62128-0383-6 | Evonik Corporation | BULK INGREDIENT | Export only | |
| Gemcitabine hydrochloride | 62128-0383-1 | Evonik Corporation | BULK INGREDIENT | Export only | |
| GEMCITABINE | 63323-125-94 | Fresenius Kabi USA, LLC | ANDA090799 | HUMAN PRESCRIPTION DRUG | ANDA |
| GEMCITABINE | 16714-909-01 | NorthStar Rx LLC | ANDA091365 | HUMAN PRESCRIPTION DRUG | ANDA |
| Gemcitabine | 0409-0181-01 | Hospira, Inc. | NDA200795 | HUMAN PRESCRIPTION DRUG | NDA |
| GEMCITABINE | 63323-102-94 | Fresenius Kabi USA, LLC | ANDA090799 | HUMAN PRESCRIPTION DRUG | ANDA |
| Gemcitabine | 0409-0182-25 | Hospira, Inc. | NDA200795 | HUMAN PRESCRIPTION DRUG | NDA |
| gemcitabine | 25021-235-50 | Sagent Pharmaceuticals | ANDA202485 | HUMAN PRESCRIPTION DRUG | ANDA |
| gemcitabine | 55390-391-50 | Bedford Laboratories | ANDA091365 | HUMAN PRESCRIPTION DRUG | ANDA |
| GEMCITABINE | 50742-497-53 | Ingenus Pharmaceuticals, LLC | ANDA210383 | HUMAN PRESCRIPTION DRUG | ANDA |
| GEMCITABINE | 50742-496-26 | Ingenus Pharmaceuticals, LLC | ANDA210383 | HUMAN PRESCRIPTION DRUG | ANDA |
| GEMCITABINE | 50742-498-05 | Ingenus Pharmaceuticals, LLC | ANDA210383 | HUMAN PRESCRIPTION DRUG | ANDA |
| Gemcitabine | 72485-222-10 | Armas Pharmaceuticals Inc. | ANDA210991 | HUMAN PRESCRIPTION DRUG | ANDA |
| GEMCITABINE | 16729-423-33 | Accord Healthcare Inc. | NDA209604 | HUMAN PRESCRIPTION DRUG | NDA |
| GEMCITABINE | 63323-126-03 | Fresenius Kabi USA, LLC | ANDA090799 | HUMAN PRESCRIPTION DRUG | ANDA |
| Gemcitabine | 0409-0185-01 | Hospira, Inc. | ANDA078339 | HUMAN PRESCRIPTION DRUG | ANDA |
| GEMCITABINE | 71288-113-10 | Meitheal Pharmaceuticals Inc. | ANDA091365 | HUMAN PRESCRIPTION DRUG | ANDA |
| Gemcitabine | 71288-117-28 | Meitheal Pharmaceuticals Inc. | ANDA212129 | HUMAN PRESCRIPTION DRUG | ANDA |
| GEMCITABINE | 68001-342-34 | BluePoint Laboratories | NDA209604 | HUMAN PRESCRIPTION DRUG | NDA |
| GEMCITABINE | 63323-125-53 | Fresenius Kabi USA, LLC | ANDA090799 | HUMAN PRESCRIPTION DRUG | ANDA |
| GEMCITABINE | 63323-126-00 | Fresenius Kabi USA, LLC | ANDA090242 | HUMAN PRESCRIPTION DRUG | ANDA |
| Gemcitabine | 72485-221-02 | Armas Pharmaceuticals Inc. | ANDA210991 | HUMAN PRESCRIPTION DRUG | ANDA |
| GEMCITABINE | 16729-391-30 | Accord Healthcare Inc. | NDA209604 | HUMAN PRESCRIPTION DRUG | NDA |
| GEMCITABINE HYDROCHLORIDE | 69097-313-37 | Cipla USA Inc. | ANDA078759 | HUMAN PRESCRIPTION DRUG | ANDA |
| Gemcitabine | 0409-0182-01 | Hospira, Inc. | NDA200795 | HUMAN PRESCRIPTION DRUG | NDA |
| Gemcitabine | 71288-117-54 | Meitheal Pharmaceuticals Inc. | ANDA212129 | HUMAN PRESCRIPTION DRUG | ANDA |
| gemcitabine | 25021-235-51 | Sagent Pharmaceuticals | ANDA202485 | HUMAN PRESCRIPTION DRUG | ANDA |
| Gemcitabine | 72485-223-20 | Armas Pharmaceuticals Inc. | ANDA210991 | HUMAN PRESCRIPTION DRUG | ANDA |
| gemcitabine | 25021-234-10 | Sagent Pharmaceuticals | ANDA202485 | HUMAN PRESCRIPTION DRUG | ANDA |
| GEMCITABINE | 63323-102-13 | Fresenius Kabi USA, LLC | ANDA090799 | HUMAN PRESCRIPTION DRUG | ANDA |
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