Ranitidine
- Product NDC
- 63629-8216
- 11-digit product format
- 636298216
- Labeler code
- 63629
- Product ID
- 63629-8216_43c4ab14-25a9-407b-8789-b63bbddb0f60
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078542
- Marketing category
- ANDA
- Marketing start
- 2008-11-19
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8216-1 | 63629821601 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8216-1) | 2019-08-14 | 0000-00-00 | No | No | Current |
| 63629-8216-2 | 63629821602 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-8216-2) | 2019-08-14 | 0000-00-00 | No | No | Current |