Drug Master Files for: Aton
✉ Email this page to a colleague
Aton Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
10330 | I | III | 7/1/1993 | WHEATON PHARMATECH | N4003-45 PINK |
11173 | I | III | 10/14/1994 | WHEATON PHARMATECH | RUBBER CLOSURE FORMULATION B5006-50 BLACK |
11752 | I | III | 11/20/1995 | WHEATON WORLDWIDE INC | PLASTIC CONTAINERS |
1180 | A | III | 5/8/1968 | KRATON POLYMERS US LLC | KRATON FG1924, G1657 MS & G1660 HU |
1352 | I | II | 4/14/1969 | PHARMATON LTD | NEO-LIDOCATION |
16096 | I | V | 8/5/2002 | PATHEON UK LTD SWINDON OPERATONS | STERILE MANUFACTURING AT SWINDON, UNITED KINGDOM. |
18513 | A | III | 7/14/2005 | WHEATON BRASIL VIDROS SA | GLASS VIALS |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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