63629-1046 : Naltrexone Hydrochloride 50 mg Oral Tablet, Film Coated
NDC: | 63629-1046 |
Labeler: | Bryant Ranch Prepack |
Product Type: | Human Prescription Drug |
Drug Name: | Naltrexone Hydrochloride |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA075274 |
Rev. Date: |
Appearance:
Markings: | EL;15 |
Shapes: |
Round |
Colors: |
Yellow |
Size (mm): | 10 |
Segments: * | 2 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces. |
NDC Package Codes:
- 63629-1046-1: 30 TABLET, FILM COATED IN 1 BOTTLE (63629‑1046‑1)
Active Ingredients:
- Naltrexone Hydrochloride
Dosage Strength:
- 50 mg
Inactive Ingredients:
- Silicon Dioxide
- Croscarmellose Sodium
- Hypromellose, Unspecified
- Hydroxypropyl Cellulose (1600000 Wamw)
- Anhydrous Lactose
- Magnesium Stearate
- Microcrystalline Cellulose
- Polyethylene Glycol, Unspecified
- Titanium Dioxide
- Ferric Oxide Yellow /
Pharmaceutical Classes:
- Opioid Antagonist [EPC]
- Opioid Antagonists [MoA]
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NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.