Tamoxifen Citrate
- Product NDC
- 70771-1185
- 11-digit product format
- 707711185
- Labeler code
- 70771
- Product ID
- 70771-1185_780b2275-d2c9-4018-890c-aeff05b32845
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamoxifen Citrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA206694
- Marketing category
- ANDA
- Marketing start
- 2018-01-03
- Marketing end
- 0000-00-00
- Substance
- TAMOXIFEN CITRATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Estrogen Agonist/Antagonist [EPC], Selective Estrogen Receptor Modulators [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70771-1185 | TAMOXIFEN CITRATE TABLET, FILM COATED [ZYDUS LIFESCIENCES LIMITED] | 6 | Legacy NDC | 20231005_70052366-80f3-41bc-b2dd-c1efe9317243.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1185-0 | 70771118500 | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1185-0) | 2018-01-03 | 0000-00-00 | No | No | Current |
| 70771-1185-1 | 70771118501 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1185-1) | 2018-01-03 | 0000-00-00 | No | No | Current |
| 70771-1185-3 | 70771118503 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1185-3) | 2018-01-03 | 0000-00-00 | No | No | Current |
| 70771-1185-6 | 70771118506 | 60 TABLET, FILM COATED in 1 BOTTLE (70771-1185-6) | 2018-01-03 | 0000-00-00 | No | No | Current |
| 70771-1185-9 | 70771118509 | 90 TABLET, FILM COATED in 1 BOTTLE (70771-1185-9) | 2018-01-03 | 0000-00-00 | No | No | Current |