NDC properties for NDC 9 0299-6100
NDC item 00299610010
NDC 9 | 0299-6100 |
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NDC 10 | 0299-6100-10 |
NDC Item | 00299610010 |
packaging | 1 TUBE in 1 CARTON (0299-6100-10) / 100 g in 1 TUBE |
FDA SPL set id | 127914 |
Labeler | Galderma Laboratories, L.P. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | NDA |
Marketing effective time low | 2006-06-29 |
Marketing status | COMPLETED |
NDA | NDA021717 |
NDC item 00299610035
NDC 9 | 0299-6100 |
---|---|
NDC 10 | 0299-6100-35 |
NDC Item | 00299610035 |
packaging | 1 TUBE in 1 CARTON (0299-6100-35) / 30 g in 1 TUBE |
FDA SPL set id | 127914 |
Labeler | Galderma Laboratories, L.P. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | NDA |
Marketing effective time low | 2006-06-29 |
Marketing status | COMPLETED |
NDA | NDA021717 |
NDC item 51672530502
NDC 9 | 51672-5305 |
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NDC 10 | 51672-5305-2 |
NDC Item | 51672530502 |
packaging | 1 TUBE in 1 CARTON (51672-5305-2) / 30 g in 1 TUBE |
FDA SPL set id | 540569 |
Labeler | Taro Pharmaceuticals U.S.A., Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | NDA |
Marketing effective time low | 2018-12-11 |
Marketing status | ACTIVE |
NDA | NDA021717 |
NDC item 73575000902
NDC 9 | 73575-009 |
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NDC 10 | 73575-009-02 |
NDC Item | 73575000902 |
packaging | 2 TUBE in 1 CARTON (73575-009-02) / 30 g in 1 TUBE |
FDA SPL set id | 500476 |
Labeler | OBA PHARMACEUTICALS INC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | NDA |
Marketing effective time low | 2020-01-24 |
Marketing status | COMPLETED |
NDA | NDA021717 |
NDC item 73575000904
NDC 9 | 73575-009 |
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NDC 10 | 73575-009-04 |
NDC Item | 73575000904 |
packaging | 4 TUBE in 1 CARTON (73575-009-04) / 30 g in 1 TUBE |
FDA SPL set id | 500476 |
Labeler | OBA PHARMACEUTICALS INC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | NDA |
Marketing effective time low | 2020-01-24 |
Marketing status | COMPLETED |
NDA | NDA021717 |
NDC item 73575000909
NDC 9 | 73575-009 |
---|---|
NDC 10 | 73575-009-09 |
NDC Item | 73575000909 |
packaging | 1 TUBE in 1 CARTON (73575-009-09) / 30 g in 1 TUBE |
FDA SPL set id | 500476 |
Labeler | OBA PHARMACEUTICALS INC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | NDA |
Marketing effective time low | 2020-01-24 |
Marketing status | COMPLETED |
NDA | NDA021717 |