NDC properties for NDC 9 0009-0085
NDC item 00009008510
NDC 9 | 0009-0085 |
---|---|
NDC 10 | 0009-0085-10 |
NDC Item | 00009008510 |
packaging | 1 VIAL in 1 CARTON (0009-0085-10) / 10 mL in 1 VIAL |
ANDA | ANDA085635 |
DCSA | CIII |
Labeler | Pharmacia & Upjohn Company LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-07-01 |
Marketing status | ACTIVE |
NDC item 00009034702
NDC 9 | 0009-0347 |
---|---|
NDC 10 | 0009-0347-02 |
NDC Item | 00009034702 |
packaging | 1 VIAL in 1 CARTON (0009-0347-02) / 10 mL in 1 VIAL |
ANDA | ANDA085635 |
DCSA | CIII |
Labeler | Pharmacia & Upjohn Company LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 1979-07-25 |
Marketing status | ACTIVE |
NDC item 76420042510
NDC 9 | 76420-425 |
---|---|
NDC 10 | 76420-425-10 |
NDC Item | 76420042510 |
packaging | 1 VIAL in 1 CARTON (76420-425-10) / 10 mL in 1 VIAL |
ANDA | ANDA085635 |
DCSA | CIII |
Labeler | Asclemed USA, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 1979-07-25 |
Marketing status | active |