NDC properties for NDC 9 0591-2114
NDC item 00591211481
NDC 9 | 0591-2114 |
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NDC 10 | 0591-2114-81 |
NDC Item | 00591211481 |
packaging | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0591-2114-81) / 90 mL in 1 BOTTLE, WITH APPLICATOR |
ANDA | ANDA205328 |
DCSA | CIII |
FDA SPL set id | 673536 |
Labeler | Actavis Pharma, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-08-18 |
Marketing status | ACTIVE |
NDC item 24979013026
NDC 9 | 24979-130 |
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NDC 10 | 24979-130-26 |
NDC Item | 24979013026 |
packaging | 1 BOTTLE, PUMP in 1 CARTON (24979-130-26) / 110 mL in 1 BOTTLE, PUMP |
ANDA | ANDA209836 |
DCSA | CIII |
FDA SPL set id | 850662 |
Labeler | Upsher-Smith Laboratories, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-12-31 |
Marketing status | ACTIVE |
NDC item 45802061001
NDC 9 | 45802-610 |
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NDC 10 | 45802-610-01 |
NDC Item | 45802061001 |
packaging | 1 BOTTLE, PUMP in 1 CARTON (45802-610-01) / 110 mL in 1 BOTTLE, PUMP |
ANDA | ANDA204255 |
DCSA | CIII |
FDA SPL set id | 700458 |
Labeler | Padagis Israel Pharmaceuticals Ltd |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-06-28 |
Marketing status | ACTIVE |
NDC item 62332048811
NDC 9 | 62332-488 |
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NDC 10 | 62332-488-11 |
NDC Item | 62332048811 |
packaging | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (62332-488-11) / 110 mL in 1 BOTTLE, WITH APPLICATOR |
ANDA | ANDA212882 |
DCSA | CIII |
FDA SPL set id | 752837 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-12-08 |
Marketing status | ACTIVE |
NDC item 63629931001
NDC 9 | 63629-9310 |
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NDC 10 | 63629-9310-1 |
NDC Item | 63629931001 |
packaging | 1 BOTTLE, PUMP in 1 CARTON (63629-9310-1) / 110 mL in 1 BOTTLE, PUMP |
ANDA | ANDA204255 |
DCSA | CIII |
FDA SPL set id | 805065 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-06-28 |
Marketing status | ACTIVE |
NDC item 66993096389
NDC 9 | 66993-963 |
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NDC 10 | 66993-963-89 |
NDC Item | 66993096389 |
packaging | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (66993-963-89) / 90 mL in 1 BOTTLE, WITH APPLICATOR |
DCSA | CIII |
FDA SPL set id | 327477 |
Labeler | Prasco Laboratories |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | NDA AUTHORIZED GENERIC |
Marketing effective time high | 2018-12-31 |
Marketing effective time low | 2017-01-23 |
Marketing status | COMPLETED |
NDA_AUTHORIZED_GENERIC | NDA022504 |
NDC item 68180094311
NDC 9 | 68180-943 |
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NDC 10 | 68180-943-11 |
NDC Item | 68180094311 |
packaging | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68180-943-11) / 90 mL in 1 BOTTLE, WITH APPLICATOR |
ANDA | ANDA208061 |
DCSA | CIII |
FDA SPL set id | 468196 |
Labeler | Lupin Pharmaceuticals, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2018-02-23 |
Marketing status | ACTIVE |
NDC item 69097036344
NDC 9 | 69097-363 |
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NDC 10 | 69097-363-44 |
NDC Item | 69097036344 |
packaging | 1 BOTTLE in 1 CARTON (69097-363-44) / 90 mL in 1 BOTTLE |
ANDA | ANDA209533 |
DCSA | CIII |
FDA SPL set id | 497849 |
Labeler | Cipla USA Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2018-03-30 |
Marketing status | ACTIVE |
NDC item 69339015810
NDC 9 | 69339-158 |
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NDC 10 | 69339-158-10 |
NDC Item | 69339015810 |
packaging | 1 BOTTLE in 1 CARTON (69339-158-10) / 110 mL in 1 BOTTLE |
ANDA | ANDA212301 |
DCSA | CIII |
FDA SPL set id | 776899 |
Labeler | NATCO Pharma USA LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time high | 2024-03-31 |
Marketing effective time low | 2021-07-12 |
Marketing status | COMPLETED |
NDC item 72162142102
NDC 9 | 72162-1421 |
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NDC 10 | 72162-1421-2 |
NDC Item | 72162142102 |
packaging | 1 BOTTLE, PUMP in 1 CARTON (72162-1421-2) / 110 mL in 1 BOTTLE, PUMP |
ANDA | ANDA204255 |
DCSA | CIII |
FDA SPL set id | 821399 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-06-28 |
Marketing status | ACTIVE |