Drug Master Files for: doxycycline hyclate
✉ Email this page to a colleague
doxycycline hyclate Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
12864 | I | II | 2/17/1998 | HENAN KAIFENG PHARMACEUTICAL FACTORY | DOXYCYCLINE HYDROCHLORIDE |
13040 | I | II | 6/25/1998 | KUNSHAN ORIENTAL PHARMACEUTICAL CO LTD | DOXYCYCLINE USP, NON-STERILE BULK DRUG |
13174 | A | II | 9/10/1998 | YANGZHOU PHARMACEUTICAL CO LTD | DOXYCYCLINE HYCLATE |
13202 | I | II | 4/30/1998 | HOUBA INC | DOXYCYCLINE HYCLATE |
13321 | I | II | 9/1/1998 | PFIZER INC | DOXYCYCLINE HYCLATE |
>DMF No. | >Status | >Type | >Submission Date | >Holder | >Subject |
Drug Master File Glossary
STATUS OF DMFS
- A = Active. This means that the DMF was found acceptable for filing, administratively, and is up-to-date.
- I = Inactive
- N = Not an assigned number
- P = DMF Pending Filing Review
TYPES OF DMFs
- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)
- Type II Drug Substance, Drug Substance Intermediate, and Material Used in Their Preparation, or Drug Product
- Type III Packaging Material
- Type IV Excipient, Colorant, Flavor, Essence, or Material Used in Their Preparation
- Type V FDA Accepted Reference Information