Tamoxifen Citrate
- Product NDC
- 63739-143
- 11-digit product format
- 637390143
- Labeler code
- 63739
- Product ID
- 63739-143_e299845a-8472-5ee4-e053-2995a90ac1f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamoxifen Citrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA075797
- Marketing category
- ANDA
- Marketing start
- 2021-12-14
- Marketing end
- 0000-00-00
- Substance
- TAMOXIFEN CITRATE
- Active strength
- 10 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-143-10 | 63739014310 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-143-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2021-12-14 | 0000-00-00 | No | No | Current |