66993-345 : Lofexidine Hydrochloride .2 mg Oral Tablet, Film Coated
| NDC: | 66993-345 |
| Labeler: | Prasco Laboratories |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Lofexidine Hydrochloride |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | NDA209229 |
| Rev. Date: |
NDC Package Codes:
- 66993-345-37: 1 BOTTLE IN 1 CARTON (66993‑345‑37) / 36 TABLET, FILM COATED IN 1 BOTTLE
- 66993-345-76: 1 BOTTLE IN 1 CARTON (66993‑345‑76) / 96 TABLET, FILM COATED IN 1 BOTTLE
Active Ingredients:
- Lofexidine Hydrochloride
Dosage Strength:
- .2 mg
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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.